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<dc:title>craigslist | science/biotech jobs in san diego</dc:title>
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<title><![CDATA[Chemical Technician  (San Diego)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1461988058.html</link>
<description><![CDATA[Sapphire Energy is a venture capital backed company developing next generation biofuels based on recent advances in metabolic engineering. The company’s focus is the commercialization of high performance, low cost, and low carbon biofuels that will substitute for conventional gasoline, diesel, and jet fuel.<br>
<br>
Job Description<br>
We seek a chemical technician to support the development of our biomass processing technology.<br>
<br>
Responsibilities<br>
•	Perform routine and experimental tasks related to extraction of oils and byproducts from biomass. <br>
•	Support R&D and engineering for scale up of extraction processes. <br>
•	Perform oil extractions on a daily basis.  Use various extraction tools such as pumps, acid-base chemistry, solvent evaporation, centrifugation etc.<br>
•	Record data and work with the analytical chemistry group for sample and data tracking.<br>
•	 Work with organic solvents, drying, distillation, filtration, liquid-liquid extractions, etc. <br>
•	Perform routine analysis such ash and moisture content, gravimetric yield, etc.<br>
•	Perform laboratory scale experiments for oil refining, degumming, bleaching, hydrolysis reactions, deodorization, vacuum distillation. <br>
•	Sample preparation for analysis and bench scale experiments<br>
•	Assisting with the harvesting of algae, flocculation and centrifugation.<br>
•	Assisting with the algae innoculation and growth in mini ponds, movement and pumping of water and media.<br>
•	Maintain laboratory space, supplies and equipment<br>
<br>
<br>
Requirements<br>
•	Bachelor’s or associate degree in chemical processing related field.<br>
•	Experience with bench scale chemical equipment.<br>
•	Experience working with organic solvents preferred.<br>
•	Due to the highly collaborative nature of this position, interpersonal and communications skills will be extremely important.<br>
<br>
Sapphire offers very competitive compensation packages (including bonuses and equity) and an attractive benefits package (health, dental, vision insurance, 401k, and paid time off). To apply, please send your CV and cover letter to human.resources@sapphirefuel.com and note Chemical Technician in the subject line.<br>
]]></description>
<dc:date>2009-11-11T16:35:45-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1461988058.html</dc:source>
<dc:title><![CDATA[Chemical Technician  (San Diego)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-11T16:35:45-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1461954759.html">
<title><![CDATA[Research Associates (2 openings)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1461954759.html</link>
<description><![CDATA[BioPhase Solutions specializes in recruiting top talented professionals for San Diego's Scientific community. We are currently looking for Research Associates to work for a leading San Diego biotechnology company. <br>
<br>
Research Associate (2 openings) <br>
<br>
Job duties include but are not limited to: <br>
<br>
-Performing routine chemical and biochemical testing <br>
-Using standard laboratory instrumentation: i.e., fluorescence plate readers, liquid handling robotics <br>
-Produce and test complex reagents <br>
-Hands-on testing and integration of – hardware, firmware, software, chemistry/reagents, and application components <br>
-Participating on multidisciplinary teams <br>
-Supporting the testing and screening of new materials <br>
-System level testing, assay testing, and image analysis <br>
-Analysis of large complex data sets <br>
-Keeping a laboratory notebook <br>
-Present updates, write reports, and conduct technical meetings <br>
<br>
Qualifications <br>
<br>
-The ideal candidate with have a BS or MS degree in Physical and or Analytical Chemistry or Physics and 1-5 years experience <br>
-Product development experience, including integration and test, transfer to production, and documentation <br>
-A sound foundation in analytical chemistry <br>
-Excellent communication skills <br>
-A desire to be part of face paced dynamic development environment <br>
 <br>
<br>
Please visit www.biophaseinc.com to view additional opportunities in San Diego County!]]></description>
<dc:date>2009-11-11T16:11:45-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1461954759.html</dc:source>
<dc:title><![CDATA[Research Associates (2 openings)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-11T16:11:45-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1461858437.html">
<title><![CDATA[Production Associate / Cell Culturist (Sorrento Valley)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1461858437.html</link>
<description><![CDATA[We are a unique biotechnology company that specializes in the development and manufacturing of biologics utilizing single-use technology to perform a vast array of process development and production projects for its client partners. <br>
<br>
We are seeking an independent, organized and energetic Production Associate to be a key member of our dynamic, fast-paced development and manufacturing team for a temporary period of approximately 3 months. <br>
<br>
The successful candidate will primarily be responsible for cell culture, dilution cloning, and analysis of stable cell clones. Addition responsibilities will include implementing production and manufacturing procedures, assisting with process improvement projects and ensuring regulatory requirements. This associate may be responsible for performing various aseptic procedures in a cGMP clean room environment both inside and outside of a biosafety cabinet depending on the level of experience. Familiarity with biopharmaceutical production processes from cell thaw, cell culture, bioreactors and harvest of unprocessed bulk is preferred. Writing development reports, protocols and batch records as well as participation in technology transfer will be required. Experience with downstream/purification processes is a plus. This associate will demonstrate strong scientific/technical and interpersonal skills as well as the ability to communicate effectively. This associate will be self motivated and able to work independently. <br>
<br>
Preferred Requirements: <br>
-B.S. in biology/life sciences or related field with 2+ yrs industrial experience in process development and cGMP manufacturing <br>
-Expertise in cell culture, purification experience a plus <br>
-Experience in manufacturing of products following SOPs, batch records and working within a cGMP regulated environment preferred<br>
-Ability to observe technical issues and assist with troubleshooting process and equipment problems as necessary <br>
-Create and review manufacturing and equipment SOPs, BRs, and reports <br>
-Maintain familiarity with regulatory requirements, cGMPs and SOPs <br>
-Work on complex assignments of diverse scope and must exercise judgment within defined procedures and practices to determine appropriate actions <br>
-Expertise in aseptic processing <br>
-Excellent record keeping and documentation skills including process records and equipment use and maintenance ]]></description>
<dc:date>2009-11-11T15:04:15-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1461858437.html</dc:source>
<dc:title><![CDATA[Production Associate / Cell Culturist (Sorrento Valley)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-11T15:04:15-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1461833453.html">
<title><![CDATA[Water Market Reseach Intern]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1461833453.html</link>
<description><![CDATA[A local water start-up is offering internships to qualified students or graduates that are seeking to hone their research and writing skills in the fast-paced and exciting atmosphere of a newly launched venture.<br>
<br>
The Company is currently developing a online application to help water utility customers save water, save money and get rewarded for their actions. <br>
<br>
Specific Objectives:<br>
<br>
- Assist in mapping the addressable market for the services offered by the Company<br>
- Reviewing and assessing online water footprint calculators<br>
- Researching and compiling information on local, state and federal water efficiency rebate programs and incentives<br>
- Researching and presenting variations in water rates throughout the US and specifically through California<br>
- Researching EPA's WaterSense Program and compile list of approved/certified products and appliances<br>
<br>
Qualified candidates will:<br>
<br>
- Be committed to sustainability and have a demonstrated understanding of local and global water scarcity issues<br>
- Have expertise in natural resources, environmental policy and/or water management<br>
- Have experience in working independently with minimal oversight and a consistent history of delivering on specific objectives <br>
- Be willing to dedicate up to 20 hours a week to the tasks and deliverables assigned.<br>
- Have a general understanding in the power of social networking/media.<br>
- Have a general understanding of rewards/loyalty programs.<br>
<br>
Keyowrds: clean technology, cleantech, venture, start-up, water, water efficiency]]></description>
<dc:date>2009-11-11T14:47:52-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1461833453.html</dc:source>
<dc:title><![CDATA[Water Market Reseach Intern]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-11T14:47:52-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1461331242.html">
<title><![CDATA[Genetic Researcher (Curator)  (Sorrento Valley)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1461331242.html</link>
<description><![CDATA[Pathway Genomics is looking for a geneticist to join our team.  We are looking for a self-motivated person whose primary responsibilities will be to extract genotype-phenotype associations from published literature.  Tasks will include identifying genetic markers (SNPs, STRs, and CNVs) which are associated with disease or ancestry, organizing extracted data into a database, and generating written reviews for specific diseases.  The successful candidate may also be involved in developing risk algorithms, writing scientific content for the website, and/or searching for background information on diseases.   Members of the team interact with assay development scientists, high-throughput screening scientists, bioinformaticists, and web developers.  <br>
Salary level depends on qualifications and experience.  Local candidates only.   <br>
Required Qualifications:<br>
•	PhD in molecular biology, genetics, or related field is required.<br>
•	Basic understanding of statistics is necessary.  Knowledge of statistics associated with genetics and/or epidemiology would be ideal.  <br>
•	The successful candidate will be detail-oriented, organized, and have excellent oral and written communication skills.  <br>
Pathway Genomics is a start-up, direct-to-consumer genetic testing company located in Sorrento Valley (San Diego).    Our mission is to empower you with the most secure, comprehensive and affordable personal genomic information available and to become your partner in utilizing that information to improve your health and wellness.<br>
<br>
<br>
]]></description>
<dc:date>2009-11-11T10:10:02-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1461331242.html</dc:source>
<dc:title><![CDATA[Genetic Researcher (Curator)  (Sorrento Valley)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-11T10:10:02-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1460980954.html">
<title><![CDATA[experienced notetaker needed (La Jolla )]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1460980954.html</link>
<description><![CDATA[Hi- there is a one day scientific conference on November 18th that needs a well organized notetaker! This is a conference dedicated to constructing an online scientific method manual that will be tremendously helpful to scientists in a variety of different fields. You should be college educated or in college now - computer literate and a good typist. It would help if you had some experience with science and / or scientific methods. This one day job could potentially lead to an opportunity to help write a scientific manual that will be posted on the internet and used by scientists all over the world. Please call 858-229-0516 or reply by email if interested. There may be some opportunity for payment and the experience will look great on a resume: <a href="http://www.selectbiosciences.com/conferences/DREAMWorkshop/"  rel="nofollow">http://www.selectbiosciences.com/conferences/DREAMWorkshop/</a> <br>
]]></description>
<dc:date>2009-11-11T06:57:40-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1460980954.html</dc:source>
<dc:title><![CDATA[experienced notetaker needed (La Jolla )]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-11T06:57:40-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1460483695.html">
<title><![CDATA[Associate Scientist(Immuno) (Mira Mesa)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1460483695.html</link>
<description><![CDATA[Leading biotech company in Mira Mesa has immediate  openings for Associate Scientists with extensive Immunology experience. This position is responsible for the manufacturing and testing products in the Immunochemicals product line. Techniques include buffer preparation, SDS-PAGE, Western Blotting, ELISA, antibody purification/conjugation and mammalian cell culture. Other duties includes: vialing, packaging and general laboratory oraganization. Qualified candidate will have a B.S. or B.A. in a life science or related field and 8-10 years actual working experience. Must be proficient in the use of computers and general laboratory equipment. Experience writing and/or revising SOPs and work instructions. Overtime required through the end of the year. Please submit your resume for immedidate consideration. Please note this is a contract position for approx 2 months. ]]></description>
<dc:date>2009-11-10T17:28:49-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1460483695.html</dc:source>
<dc:title><![CDATA[Associate Scientist(Immuno) (Mira Mesa)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-10T17:28:49-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1460481893.html">
<title><![CDATA[Office and Accounting Administrator]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1460481893.html</link>
<description><![CDATA[Growing Biotechnology Company in North Torrey pines Rd is looking for a motivated, self starting and experienced individual to assist in a variety of accounting and administrative office functions, They must have excellent computer skills in Microsoft Office programs. Should be able to type 30-40 words a minute. Must have excellent written and oral communication skills. Positive attitude is a must!
<br>
: 
<br>
Advance knowledge with Excel 
<br>
Must be able to Generate monthly statements, P&Ls and Balance sheets 
<br>
Must be very detail orientated, willing to learn. 
<br>
Experience with QuickBooks 
<br>
Filing 
<br>
Experienced in general office 
<br>
Strong organizational skills and VERY detail oriented 
<br>
Good communication and people skills necessary 
<br>

<br>
This is a part-time job. 
<br>
]]></description>
<dc:date>2009-11-10T17:27:28-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1460481893.html</dc:source>
<dc:title><![CDATA[Office and Accounting Administrator]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-10T17:27:28-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1460403714.html">
<title><![CDATA[Postdoctoral Associate- Cell Biology (La Jolla, CA)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1460403714.html</link>
<description><![CDATA[Burnham Institute for Medical Research, an independent, non-profit, public-benefit basic research organization, located in La Jolla, California, is seeking a Postdoctoral Associate to join the research laboratory of Dr. Robert Margolis. <br>
<br>
The Margolis laboratory analyzes the specific molecular requirements for maintenance of the mitotic state.  Cell and molecular biology approaches are used to understand the mechanisms of mitotic checkpoint control, mitotic protein function, cell cleavage control and other cell cycle regulation by the cytoskeleton, principally in mammalian cells in culture.  <br>
<br>
Candidates must have a Ph.D. or equivalent, with training in cell and molecular biology including previous experience with Immunofluorescence microscopy, including time-lapse; flow cytometry; standard molecular biology techniques including viral transfection and shRNA knockdown procedures.  Prior experience in protein preparation from cell extracts, FPLC and/or HPLC column analysis, standard cell biology techniques is also required.  Familiarity with yeast or Xenopus eggs is preferred.  Candidates with a Biochemical background are also encouraged to apply.   Interested applicants should submit a single PDF file containing CV, a brief description of research accomplishments, interests, and career goals, and contact information (e-mail address and phone number) of three references to Dr. Robert Margolis (rmargolis@burnham.org). <br>
<br>
Burnham Institute for Medical Research offers a competitive compensation and benefit package. Become part of a team where Community, Compassion, Communication, Collaboration and our Commitment to Science are part of everyone's job.  Please visit www.burnham.org for additional information. <br>
Burnham Institute for Medical Research is an equal opportunity employer.<br>
]]></description>
<dc:date>2009-11-10T16:28:28-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1460403714.html</dc:source>
<dc:title><![CDATA[Postdoctoral Associate- Cell Biology (La Jolla, CA)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-10T16:28:28-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1460351684.html">
<title><![CDATA[Research Coordinator II (San Diego, CA)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1460351684.html</link>
<description><![CDATA[The Veterans Medical Research Foundation (VMRF) is a private not-for-profit medical research corporation, providing support for biomedical and health services research.<br>
<br>
<b>Qualifications Summary:</b><br>
Bachelor's degree (BA/BS) from an accredited four-year college or university in a related field and two to four years related experience and/or training; or equivalent combination of education and experience. Must provide own vehicle, and maintain a current, valid CA driver’s license and current, valid vehicle insurance.<br>
<br>
<b>Job Description Summary:</b><br>
Will coordinate all aspects of the San Diego component of a four-site intervention study evaluating medication and psychotherapeutic treatments for complicated grief. Will oversee and assist with recruitment, screening, and evaluation of participants. Will participate in regular conference calls with other site coordinators at institutions across the country to review recruitment and retention strategies, with particular attention to Hispanic-American participants in San Diego. Will interface with the investigators, staff, and participants’ primary care physicians as necessary. Will participate in weekly research meetings to review participants’ progress through the protocol and contribute to written research reports and manuscripts, including those prepared for the Data Safety Monitoring Board and the UCSD Institutional Review Board. Will supervise independent evaluators and students assigned to research project. Must be willing to travel to various locations within San Diego County and use own vehicle. May perform additional duties as required.<br>
<br>
EOE.  Please, no phone calls.<br>
<b>To apply for this position, please use the following link:</b><br>
<a href="http://tbe.taleo.net/NA7/ats/careers/requisition.jsp?org=VETERANS_MEDICAL_RESEARCH_FOUN&amp;cws=1&amp;rid=113"  rel="nofollow">http://tbe.taleo.net/NA7/ats/careers/requisition.jsp?org=VETERANS_MEDICAL_RESEARCH_FOUN&cws=1&rid=113</a>]]></description>
<dc:date>2009-11-10T15:50:04-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1460351684.html</dc:source>
<dc:title><![CDATA[Research Coordinator II (San Diego, CA)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-10T15:50:04-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/nsd/sci/1460091112.html">
<title><![CDATA[Production Technician (Carlsbad)]]></title>
<link>http://sandiego.craigslist.org/nsd/sci/1460091112.html</link>
<description><![CDATA[North County Biotech Company has an opening for a conscientious, detailed-oriented person to assist in the manufacturing of human blood/serum controls and similar products in an FDA/ISO environment.<br>
<br>
Responsibilties will include all aspects of production including formulation, analysis, documentation, filling and kit assemblies.<br>
<br>
Minimum Qualifications:<br>
* Bachelor's Degree in a relevant science<br>
* Meticulous attention to detail<br>
* Good math and computer skills<br>
* Experience in In Vitro diagnostics or clinical chemistry a plus<br>
* Eagerness to learn<br>
* Able to work in team environment<br>
<br>
Possible work shifts.<br>
<br>
Apply for this Production Technician position by emailing your resume with salary requirements / history.  <br>
]]></description>
<dc:date>2009-11-10T13:03:56-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/nsd/sci/1460091112.html</dc:source>
<dc:title><![CDATA[Production Technician (Carlsbad)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-10T13:03:56-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/nsd/sci/1459988990.html">
<title><![CDATA[Production Manager (Carlsbad)]]></title>
<link>http://sandiego.craigslist.org/nsd/sci/1459988990.html</link>
<description><![CDATA[Small North County Biotech Company has an opening for a detailed-oriented, conscientious person to supervise multiple production teams responsible for serum processing and the manufacture of lyophilized and liquid controls and calibrators.  Will supervise 3 Production teams.<br>
<br>
RESPONSIBILITIES will include:<br>
+ Manage small production staff <br>
+ Plasma / Serum processing<br>
+ Control / calibrator manufacture:<br>
    * compounding<br>
    * filtration<br>
    * centrifugation<br>
    * lyophilization<br>
    * product filling<br>
+ Writing of production documentation<br>
+ Requesting and ordering supplies and raw materials<br>
+ Manufacturing and shift scheduling<br>
+ Review customer specifications<br>
<br>
MINIMUM QUALIFICATIONS<br>
+ B.S. Biology, Chemistry, Microbiology, Biochemistry or similar degree<br>
+ Minimum two years experience in the In Vitro Diagnostic industry manufacturing reagents, control sera, lyophilized and liquid controls and calibrators<br>
+ Supervisory experience a MUST<br>
+ Good organizational skills important<br>
+ Focused<br>
+ Exceptional math skills a MUST<br>
+ Able to multi-task important<br>
+ Outgoing<br>
+ Good computer skills - MS Office and/or Open Office<br>
+ Career oriented<br>
<br>
]]></description>
<dc:date>2009-11-10T12:05:44-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/nsd/sci/1459988990.html</dc:source>
<dc:title><![CDATA[Production Manager (Carlsbad)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-10T12:05:44-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1458759526.html">
<title><![CDATA[Scientist, Assay Development (San Diego)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1458759526.html</link>
<description><![CDATA[We are a San Diego based biotech seeking a Scientist, Assay Development (PCR Expert) <br>
<br>
We have an immediate opportunity for a PCR expert in the Assay Development group for PCR assay development and validation for GLP and Clinical use. This person will be responsible to independently develop, qualify and validate in house and customer real-time PCR and multiplex PCR assays to measure gene expression, copy number, genotype, translocations and other molecular characteristics of RNA or DNA, which will be used in clinical and pre-clinical quantitative and qualatitative biomarker and companion diagnostic studies. He/she will independently perform assay design, establish assay development and validation protocol and carry out experiments; be responsible for accurate testing, documentation of results, and evaluation and analysis of data; provides technical and theoretical support to testing staff within area of specialty; researches and implements new methods and technologies to enhance operations; suggests improvements to existing methods and procedures; offers novel approaches and troubleshooting to solve complex technical problems; trains staff in scientific method and testing technologies; employs high level technical expertise to develop new techniques and creatively solve problems; reliably writes and executes well defined SOPs; interacts with clients to understand the project scope and prepares complex and detailed reports; complete other duties as assigned by supervisor. <br>
<br>
Requirements: A bachelor degree with 12 years PCR/molecular biology related industrial experience, a master degree with 9 years experience or a Ph.D. degree with 3 years experience. Detailed knowledge of PCR assay development and validation at clinical level and a minimum of 3 years proven experience in PCR assay development and validation is required. Familiarity with regulatory guidance on analytical testing and clinical molecular biology lab working experience is highly desired. Experience with assay development using FFPE fixed tissue samples is a plus. Demonstrated ability to understand and apply complex technical concepts to assay development methodology; detail oriented and strong written and verbal communication skills; ability to work independently, within prescribed guidelines, and as a team member; ability to follow detailed directions in a laboratory environment. <br>
]]></description>
<dc:date>2009-11-09T15:47:32-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1458759526.html</dc:source>
<dc:title><![CDATA[Scientist, Assay Development (San Diego)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-09T15:47:32-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1458325304.html">
<title><![CDATA[Adventurous Biologist (Alaska)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1458325304.html</link>
<description><![CDATA[Now accepting applications for the November 30th training!<br>
<br>
Adventurous Biologist to observe and sample catches onboard commerical fishing boats off Alaska.<br>
While onboard, biologists identify fish species, collect and record length, quantity, determine sex for species caught.<br>
Opportunities year round. Three week training provided.<br>
<br>
Requirements: BS degree in Biology or natural sciences, college level of Statistics and a flexible attitude, ability to pass a physical exam and<br>
be a U. S. Citizen.<br>
Please submit a current resume, Groundfish application that is available on our website at www.saltwaterinc.com, as well as the criminal convictions form and an unofficial copy of transcripts showing a minimum of 30 Biology credits.<br>
<br>
Fax to Yani at 907-258-5999, or email to yani@saltwaterinc.com.<br>
<br>
If you have any questions please feel free to call Yani at 1-800-770-3241 or 907-276-3241.<br>
]]></description>
<dc:date>2009-11-09T11:27:39-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1458325304.html</dc:source>
<dc:title><![CDATA[Adventurous Biologist (Alaska)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-09T11:27:39-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1456487189.html">
<title><![CDATA[Senior Imaging Analysis Specialist (San Diego)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1456487189.html</link>
<description><![CDATA[Our Imaging Specialist will work in tandem with our sales teams to manage and deliver high quality technical support. Our Imaging Specialist will demonstrate, promote and install imaging and capital equipment for health care, pharmaceutical and research markets. Identify customers, configure custom systems, manage pre-sales demonstration, coordinate installations, and train. <br>
<br>
Education:  Science Educational Background - MS or PhD Preferred <br>
<br>
40% - 50% travel<br>
<br>
Duties and Experience: <br>
<br>
Work in conjunction with our Sales Team to make imaging system sales. <br>
Configure customized imaging systems. <br>
Perform customer demonstrations with microscopy, pathology imaging systems, <br>
telepathology, whole slide imaging. <br>
Install, train, and support new installations. <br>
Help troubleshoot hardware and software problems. <br>
Attend 5-10 trade shows per year. <br>
Knowledge of Algorithms Processing <br>
Understand image analysis tools <br>
Experience Histology/Pathology applications <br>
Strong verbal and witting skills <br>
Image Analysis background in a Medical or Clinical Setting <br>
 <br>
Knowledge of IHC workflow <br>
Knowledge of CLIA, CAP and GLP guidelines is a plus <br>
<br>
]]></description>
<dc:date>2009-11-08T05:39:01-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1456487189.html</dc:source>
<dc:title><![CDATA[Senior Imaging Analysis Specialist (San Diego)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-08T05:39:01-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/nsd/sci/1456479908.html">
<title><![CDATA[Senior Imaging Analysis Specialist (San Diego)]]></title>
<link>http://sandiego.craigslist.org/nsd/sci/1456479908.html</link>
<description><![CDATA[Our Senior Imaging Specialist will work in tandem with our sales teams to manage and deliver high quality technical support. Our Senior Specialist will demonstrate, promote and install imaging and capital equipment for health care, pharmaceutical and research markets. Identify customers, configure custom systems, manage pre-sales demonstration, coordinate installations, and train.  40% - 50% travel.<br>
Science Educational Background - MS or PhD Preferred <br>
 <br>
Duties and Experience: <br>
<br>
Configure customized imaging systems. <br>
Perform customer demonstrations with microscopy, pathology imaging systems, <br>
telepathology, whole slide imaging. <br>
Quote imaging systems and close imaging systems sales. <br>
Install, train, and support new installations. <br>
Troubleshoot hardware, software, and optical problems. <br>
Attend 5-10 trade shows per year to demonstrate imaging systems. <br>
Digital Pathology-Image Analysis Experience<br>
Knowledge of Algorithms Processing <br>
Understand image analysis tools <br>
Strong verbal and witting skills <br>
Image Analysis background in a Medical or Clinical Setting <br>
<br>
Knowledge of IHC workflow <br>
Knowledge of CLIA, CAP and GLP guidelines is a plus <br>
<br>
<br>
]]></description>
<dc:date>2009-11-08T05:25:17-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/nsd/sci/1456479908.html</dc:source>
<dc:title><![CDATA[Senior Imaging Analysis Specialist (San Diego)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-08T05:25:17-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1454870801.html">
<title><![CDATA[Product Team Associate- Molecular Biology- Competitive Salary! (San Diego, CA)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1454870801.html</link>
<description><![CDATA[Our San Diego Life Science clients, successful leaders in the Biotechnology industry sector, have a number of excellent job openings.<br>
<br>
<br>
If you have some or all of the following cell or molecular biology techniques then Lab Support, a division of On Assignment, would love to speak with you<br>
<br>
•           High throughput cloning<br>
•           Fermentations<br>
•           Protein purification and expression <br>
•           Experience of RNA +/or DNA manipulation<br>
•           PCR techniques<br>
•           Sequencing<br>
•           Site directed mutagenesis<br>
•           GPCR second messenger assays<br>
•           High throughput screening<br>
•           Isolation and purification nucleic acid techniques<br>
•           Hands-on experience of mammalian cell culture/ recombinant cell lines<br>
 <br>
Job Requirements:<br>
BS/MS in biology along with experience of some or all of the skills listed above: <br>
<br>
Experience levels include 1-4 years of industry/academic experience. Competitive salary offered.<br>
<br>
At this time, only LOCAL candidates will be considered. For confidential consideration, please forward your resume to sandiego@labsupport.com . Thank you and we look forward to hearing from you.<br>
]]></description>
<dc:date>2009-11-06T16:41:12-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1454870801.html</dc:source>
<dc:title><![CDATA[Product Team Associate- Molecular Biology- Competitive Salary! (San Diego, CA)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-06T16:41:12-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/nsd/sci/1454838785.html">
<title><![CDATA[QA Document Coordinator (Rancho Bernardo)]]></title>
<link>http://sandiego.craigslist.org/nsd/sci/1454838785.html</link>
<description><![CDATA[Located in beautiful San Diego, our company is a growing, state of the art clinical testing laboratory providing drug testing services for physicians nationwide.  We offers a competitive salary and benefits, a positive work environment and the opportunity to work with a highly motivated and talented staff.  <br>
<br>
<br>
<br>
Title:		QA Document Coordinator<br>
<br>
Category:	Operations – Clinical Laboratory<br>
<br>
Description:	Summary<br>
The QA Document Coordinator provides support for document control and records management which includes assigning numbers, document change management, routing for review and approval; tracking all stages of routing, approval, distribution, archival of history files, maintenance of documentation and filing of all master documents. Ensure ongoing and timely support of document management, and administrative support of QA tasks including training.<br>
<br>
		Essential Duties and Responsibilities include the following:<br>
•	Responsible for Standard Operating Procedure (SOP) development and updates<br>
•	Format and edit documents, including Standard Operating Procedures (SOPs), specifications, controlled forms and policies that support the laboratory operations and comply with GLP and FDA guidelines as applicable and other quality standards<br>
•	Provide consistent document format to achieve uniformity of all clinical operations documents<br>
•	Tracks, trends and evaluates data and provides detailed reports to management for evaluation<br>
•	Strict attention to detail<br>
•	Must be flexible, able to multi-task in a fast paced environment, and operate well in a team setting<br>
•	Must be able to proof work and identify non-standard format or working, and errors within documents<br>
•	Must have the ability to facilitate training sessions; maintains training records<br>
•	May schedule and track quality assurance audits and findings; effectively communicate written and oral findings to management<br>
•	Perform all responsibilities in accordance with company policies, SOPs and with all regulatory standards and regulations<br>
•	Required to follow all safety procedures, policies, precautions, and Quality Assurance<br>
•	Other duties as assigned.<br>
<br>
Requirements:	EDUCATION and/or EXPERIENCE:<br>
Position generally requires a Bachelors degree in Life Sciences or related area, or related experience and/or training.<br>
•	Minimum 2 years directly/related experience in an equivalent role within a FDA regulated pharmaceutical or laboratory is required<br>
•	Knowledge of document control processes, working with an Electronic Document Management System is a must<br>
•	Knowledge of GLP, Quality System Regulations and ISO standards preferred<br>
•	Must be highly skilled in Microsoft Office – Word, Outlook, Excel, Access, PowerPoint and experienced with PCs and databases<br>
•	Must have excellent communication skills, with the ability to interact appropriately with all levels of management and staff<br>
•	Experience working in a high complexity CLIA/CAP environment preferred<br>
<br>
CERTIFICATES, LICENSES, REGISTRATIONS<br>
N/A<br>
<br>
If you are interested and available, please send your resume, salary history and cover letter immediatley.<br>
<br>
NO STAFFING FIRMS!!!!!!]]></description>
<dc:date>2009-11-06T16:15:50-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/nsd/sci/1454838785.html</dc:source>
<dc:title><![CDATA[QA Document Coordinator (Rancho Bernardo)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-06T16:15:50-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/nsd/sci/1454831953.html">
<title><![CDATA[Clinical Services Clerk  (Carlsbad)]]></title>
<link>http://sandiego.craigslist.org/nsd/sci/1454831953.html</link>
<description><![CDATA[Genoptix, Inc. is a fast-growing clinical laboratory focused on a complete offering of diagnostic medical services for patients with blood cancers. Currently, we have an open position in our Carlsbad, CA facility for a Clinical Services Clerk.<br>
<br>
Summary<br>
 <br>
We are currently seeking Clinical Services Clerk to deliver stained pathology slides to Hematopathologists for review daily and perform clerical duties such as filing, typing, data entry, copying documents, distribution of mail and reports.<br>
 <br>
Essential Duties & Responsibilities:<br>
Note: Other duties may be assigned. <br>
- Pickup, distribution, filing and retrieval of pathology slides and folders. <br>
- Performs clerical duties such as filing, typing, faxing, and copying documents. <br>
- Data entry.<br>
- Communication with partner laboratories to troubleshoot and correct any identified slide issues. <br>
- Handling miscellaneous pathologist requests.<br>
<br>
Qualifications:<br>
-  Excellent communication skills necessary to deal effectively with co-workers. <br>
- Ability to deal effectively with all levels of staff and to communicate clearly and concisely over the telephone.  <br>
- Willingness to work in fast paced, high volume environment.  <br>
- Able to perform written communication and data entry. <br>
- Ability to work on Saturdays. <br>
<br>
Education and/or Experience:<br>
- Requires a high school diploma or its equivalent <br>
- One to two years related experience, healthcare environment preferred. <br>
- Computer knowledge, including Microsoft applications (Word, Power Point and Excel). <br>
<br>
To be considered for this position, please apply online via the following link:<br>
<br>
<a href="http://tbe.taleo.net/NA4/ats/careers/requisition.jsp?org=GENOPTIX&cws=1&rid=393"  rel="nofollow">http://tbe.taleo.net/NA4/ats/careers/requisition.jsp?org=GENOPTIX&cws=1&rid=393</a><br>
]]></description>
<dc:date>2009-11-06T16:10:37-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/nsd/sci/1454831953.html</dc:source>
<dc:title><![CDATA[Clinical Services Clerk  (Carlsbad)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-06T16:10:37-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1454630932.html">
<title><![CDATA[Packaging Lab Technician (Sorrento Valley)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1454630932.html</link>
<description><![CDATA[This position will be responsible to fill, label and bag vials of antibody solutions.  Will also enter label info and generate vial labels.  Be able to use of pipette, scale and other packaging equipment as required.  Other duties include completing batch records, and entering and processing packaging data into database.  May also write SOPs for new packaging procedures and review and edit existing SOPs to reflect changes in procedures.  
<br>

<br>
The position requires a minimum of college coursework in Biology, Bioengineering, Biochemistry, Immunology or related studies.  Minimum 1 year of relevant experience in a laboratory and/or biotech manufacturing and/or filling/bottling/packaging working environment required, including pipetting and use of sterile technique.  Must able to work in fast environment.  Good organizational skills with ability to prioritize task.  Must be self-motivated and dependable, and able to work with minimal supervision and pay close attention to details.  Good verbal and written communication skills.  Must have the ability and knowledge to perform math calculations and measurement conversions.  Must be able to lift 30-40 lbs. unassisted.  
<br>

<br>
<b> All qualified candidates must apply and submit resume online on the Careers page of our website: www.biolegend.com </b>]]></description>
<dc:date>2009-11-06T13:50:21-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1454630932.html</dc:source>
<dc:title><![CDATA[Packaging Lab Technician (Sorrento Valley)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-06T13:50:21-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1454627991.html">
<title><![CDATA[Research Associate - Tissue Culture I or II   (San Diego)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1454627991.html</link>
<description><![CDATA[Company Overview: BioLegend develops and manufactures world-class, cutting-edge antibodies and reagents for biomedical research, offered at an outstanding value. Our product areas include cell immunophenotyping, cytokines and chemokines, adhesion, cancer research, T regulatory cells, stem cells, innate immunity, cell-cycle analysis, apoptosis, and modification-specific antibodies. All of BioLegend’s reagents are supported by superior customer service and come with a quality guarantee. Our aggressive product development program, through technology licensing, collaborations, and internal hybridoma development, produces strategic reagents for use in a variety of applications including flow cytometry, ELISA, immunoprecipitation, Western blotting, immunofluorescence microscopy, immunohistochemistry, and in vitro or in vivo functional assays. BioLegend offers the broadest selection of fluorochrome conjugates for multi-color flow cytometry. 
<br>
 
<br>
Requirements:  This position should have understanding of all aspects of hybridoma production process, will perform antibody production and troubleshooting with the new or established hybridoma cell lines. The applicant should have hands-on experience with cell line treatment, cloning/subcloning, banking, small and large scale antibody production.  
<br>

<br>
Qualifications:  BS degree in biological science is required, must have basic understanding of general Immunology, a minimum of 1-5 years experience in the areas of mammalian cell culture, antibody production, and ELISA screening assays, as well as a superb sterile technique are required. 
<br>

<br>
Strong organizational, documentation, and communication skills are essential. 
<br>

<br>
Must have a good work ethics, must be willing to work hard and dedicated. 
<br>

<br>
Must be a self-starter, flexible, highly motivated, and dependable. 
<br>

<br>
Must have problem solving and analytical skills, will be able to work independently as well as in a team environment.  
<br>
    
<br>
Interested candidates submit resume and apply online www.biolegend.com]]></description>
<dc:date>2009-11-06T13:48:33-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1454627991.html</dc:source>
<dc:title><![CDATA[Research Associate - Tissue Culture I or II   (San Diego)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-06T13:48:33-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1454328925.html">
<title><![CDATA[Lab Manager (Torrey Pines)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1454328925.html</link>
<description><![CDATA[Astute Medical Incorporated, an innovative early-stage medical diagnostics company, is seeking a part-time (32 hours/week) laboratory manager experienced in blood banking and sample inventory.  Preferred candidates should be available to work 5 days part time per week.  <br>
<br>
Requirements:  1-3 years experience in blood banking and sample inventory, computer literate (EXCEL, Word, some database experience), attentive to detail and deadline oriented, knowledgeable of handling biohazardous materials, and a college degree.<br>
<br>
Please submit your resume or curriculum vitae to us at the address below. Be sure to specify job reference ID# 355015 in the subject of the message. <br>
<br>
Email: jobs@astutemedical.com <br>
Fax: (858) 882-0449 <br>
Address: Human Resources – Astute Medical, 3550 General Atomics Court, MS 02/643, San Diego, CA 92121<br>
]]></description>
<dc:date>2009-11-06T10:56:45-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1454328925.html</dc:source>
<dc:title><![CDATA[Lab Manager (Torrey Pines)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-06T10:56:45-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/nsd/sci/1454235417.html">
<title><![CDATA[Manufacturing Associate - TEMP (Carlsbad)]]></title>
<link>http://sandiego.craigslist.org/nsd/sci/1454235417.html</link>
<description><![CDATA[Advanced Brain Monitoring, Inc. (ABM), located in North San Diego County, has a unique diversification of Department of Defense contracts, National Institute of Health grants and medical device manufacturing.  ABM is seeking a Manufacturing Associate to fill a temporary position.<br>
<br>
This temporary position is open for approximately 3-5 months with hours varying between 10-40 hours per week.  This individual must be detail oriented, very well organized, a team player and able to handle multiple tasks at once.  <br>
<br>
Our ideal candidate will have relevant experience in the following categories: <br>
•	Assembly and testing of electronics in a manufacturing environment.<br>
•	Following written instructions for manufacturing processes.<br>
•	Usage of computers for testing of electronic devices.<br>
•	Maintenance of quality system documentation for manufacturing.<br>
<br>
Duties will include assembly, testing, and documentation for medical device manufacturing.  <br>
<br>
Pay is commensurate with experience, $12-$15 hour.<br>
<br>
Please email resume to jmartin@b-alert.com<br>
]]></description>
<dc:date>2009-11-06T10:06:38-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/nsd/sci/1454235417.html</dc:source>
<dc:title><![CDATA[Manufacturing Associate - TEMP (Carlsbad)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-06T10:06:38-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1454122583.html">
<title><![CDATA[Sr. Research Associate - Pharmacology]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1454122583.html</link>
<description><![CDATA[BioPhase Solutions specializes in recruiting top talented professionals for San Diego's Scientific community. We are currently looking for a Sr. Research Associate - Pharmacology to work for a leading San Diego biotechnology company.<br>
<br>
Sr. Research Associate - Pharmacology<br>
<br>
Description: <br>
<br>
The position is within the Pharmacology Dept in the Experimental Therapeutics Group. The successful candidate will work with senior scientists to design, plan and execute in vivo studies focused on identifying drug candidates within the area of oncology. Additional responsibilities include data analysis, presentation of data to multidisciplinary discovery teams, participation in the evaluation of new targets and preparation of reports.  <br>
<br>
Qualifications: <br>
<br>
The position requires a BS in Biology or related discipline plus 5 years of industrial or relevant academic experience or MS degree with 2 years of experience. Successful candidate must have hands-on experience in evaluating small molecules in in vivo oncology models and must be proficient in animal handling, dosing, sample preparation, experimental design and data analysis. Hands-on experience in ELISA, western blots or histology is preferred. Familiarity with transgenic models, Xenogen imaging or ultrasound is desired.  The candidate should have excellent written and oral communication skills and the ability to work in a fast-paced, team-oriented drug discovery environment. <br>
<br>
Please be sure to visit www.biophaseinc.com to view additional opportunities in San Diego County!]]></description>
<dc:date>2009-11-06T09:07:48-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1454122583.html</dc:source>
<dc:title><![CDATA[Sr. Research Associate - Pharmacology]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-06T09:07:48-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/nsd/sci/1454038042.html">
<title><![CDATA[SR. SCIENTIST LV III]]></title>
<link>http://sandiego.craigslist.org/nsd/sci/1454038042.html</link>
<description><![CDATA[<p><font size="2">

<p><span style="FONT-FAMILY: Arial"><font color="#33cc33"><font color="#0066cc">At Abbott, we provide the perspectives and experience necessary to translate science into real solutions for patients in over 130 markets worldwide. Today, 72,000 Abbott employees are doing work that matters.</font></font></span></p>

</font></p>

<p>PRIMARY FUNCTION:
- 	Conceives, plans, designs, and conducts advanced independent research.
- 	Investigates and develops new procedures.
- 	Direction provided by project goals and experimental design.
- 	May act as project leader, lead scientist, or independent reviewer.
- 	Provides technical direction and feedback to others.
- 	Interacts with other groups and shares information; participates in team activities.

<p>EXPERTISE AND PROBLEM-SOLVING RESPONSIBILITIES:<br>
- 	Responsible for implementing and maintaining the effectiveness of the quality system.<br>
- 	Understands and consistently follows documented procedures.<br>
- 	Determines priorities for experiments.<br>
- 	Applies quantitative methods: analyzes data, evaluates results, forms conclusions, and provides/implements process or document improvements.<br>
- 	Independently designs and executes a series of experiments to test hypotheses related to project outcomes.<br>
- 	Applies advance scientific knowledge to projects.<br>
- 	Utilizes DOE where appropriate.<br>
- 	May assist in the design of experiments for others.<br>
- 	Identifies technical alternatives from literature review.<br>
- 	Applies basic computer skills (includes word processing, spreadsheets, instrumentation-related and Abbott network systems).<br>
- 	Produces reports and documents utilizing advanced writing skills.<br>
- 	Utilizes multiple analytical instruments; trains others in their operation.<br>
- 	Recognizes and resolves technical problems.</p>

<p>LEVEL OF ACCOUNTABILITY:<br>
Scope: Across functional areas<br>
- 	Defines project goals and is responsible for timely project completion.<br>
- 	Responsible for own Redbook documentation, and for the accuracy, quality, and timeliness of experimental results.<br>
- 	Summarizes data and analyzes results, independently formulates conclusions, and determines future experiments.<br>
- 	Actively participates in routine maintenance, lab safety; may assume roles of responsibility, such as training or document control.</p>

<p>LEADERSHIP ACTIVITIES:<br>
- 	Prepares results of projects internally and may present externally.<br>
- 	Reviews, evaluates, and critiques presentations for others.<br>
- 	Presents complex technical data to large and diverse groups.<br>
- 	Trains others on the theoretical and practical basis of techniques, processes, and assays.<br>
- 	Participates in project planning, updates, and process improvements.<br>
- 	May generate new product ideas consistent with division strategy.<br>
- 	Prepares and aligns goals with manager's goals.<br>
- 	May coach lower-level scientists (e.g., presentation skills, negotiation skills, decision-making, and contingency planning).<br>
- 	Influences decision-making through negotiation, addressing conflict, and by building (productive) working relationships across functional areas.</p>

<p>INTERPERSONAL SKILLS:<br>
- 	Participate in technology teams.<br>
- 	Develop and maintain internal and external customer contacts to maintain technical knowledge as required to accomplish objectives.</p>

<p><b>QUALIFICATIONS:</b></p>

<p>Basic Qualifications:</p>

<p>Knowledge of regulations and standards affecting IVDs and Biologics.</p>

<p>Position may be graded B5/B6 based on candidate's skills/experience level.</p>

<p>Preferred Qualifications:</p>

<p><font color="#33cc00" size="2">

<p><span style="FONT-FAMILY: Arial"><span style="FONT-FAMILY: Arial"><font color="#0066cc">Through numerous local, national and international accolades, Abbott is regarded as an employer of choice for our commitment to workplace excellence. Our employees are given the tools to succeed, lead and grow, with challenging opportunities and work that makes a difference. Through our diverse healthcare businesses, we connect people and potential in ways that no other company can. </font></span></span></p>

<p><span style="FONT-FAMILY: Arial"><font color="#0066cc">Discover a world of opportunities at Abbott. </font></span></p>

<p><font color="#0066cc"><span style="FONT-FAMILY: Arial">&nbsp;</span><strong style="mso-bidi-font-weight: normal"><span style="FONT-FAMILY: Arial"><em>EEO Statement: </em></span></strong></font></p>

<p><span style="FONT-FAMILY: Arial"><em><font color="#0066cc">At Abbott, we believe that diversity drives innovation. Innovative thinkers who are passionate about the work they do, Abbott employees are representative of the diversity of the patients we strive to serve every single day across the globe.</font></em></span></p>

</font>

<br>
<br>
If interested, please apply online at <a href="http://track.jobviper.com/ViewJob.asp?id=649797-1432-6418"  rel="nofollow">http://track.jobviper.com/ViewJob.asp?id=649797-1432-6418</a>
]]></description>
<dc:date>2009-11-06T08:21:39-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/nsd/sci/1454038042.html</dc:source>
<dc:title><![CDATA[SR. SCIENTIST LV III]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-06T08:21:39-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/nsd/sci/1454036030.html">
<title><![CDATA[ PRINCIPAL SCIENTIST II (Carlsbad, CA)]]></title>
<link>http://sandiego.craigslist.org/nsd/sci/1454036030.html</link>
<description><![CDATA[<p><font size="2">

<p><span style="FONT-FAMILY: Arial"><font color="#33cc33"><font color="#0066cc">At Abbott, we provide the perspectives and experience necessary to translate science into real solutions for patients in over 130 markets worldwide. Today, 72,000 Abbott employees are doing work that matters.</font></font></span></p>

</font></p>

<p><font size="1"><strong>PRIMARY FUNCTION:<br>
</strong></font><font face="Helv"><font face="Helv" size="1"><strong><strong><font face="Helv" size="1"><font face="Helv" size="1"><br>
-&nbsp;&nbsp; Conceives, designs, conducts and leads advanced independent or multi-disciplinary research driven by strategic business needs.<br>
-&nbsp;&nbsp; Provides technical review of experimental results.<br>
-&nbsp;&nbsp; Serves as a technical role model to others.&nbsp;<br>
-&nbsp;&nbsp; Provides consultation to others on technical issues.<br>
-&nbsp;&nbsp; Interacts with other groups and shares information; participates in team activities.</font></font><br>
<br>
EXPERTISE AND PROBLEM-SOLVING RESPONSIBILITIES:<br>
<strong><font face="Helv" size="1"><font face="Helv" size="1">-&nbsp;&nbsp; Responsible for implementing and maintaining the effectiveness of the quality system.<br>
-&nbsp;&nbsp; Understands and consistently follows documented procedures.<br>
-&nbsp;&nbsp; Identifies/communicates to other areas in the division implications of relevant scientific observations.&nbsp;<br>
-&nbsp;&nbsp; Conceives, plans, and executes projects related to the strategic needs of the division.<br>
-&nbsp;&nbsp; Independently designs and executes a series of experiments to test hypotheses related to project outcomes.<br>
-&nbsp;&nbsp; Applies advance scientific knowledge to projects.<br>
-&nbsp;&nbsp; Utilizes DOE where appropriate.<br>
-&nbsp;&nbsp; Ensures quality through sound experimental design, execution and evaluation.<br>
-&nbsp;&nbsp; Assists in the design of experiments for others.<br>
-&nbsp;&nbsp; Identifies new directions for research from literature review.<br>
-&nbsp;&nbsp; Applies basic computer skills (includes word processing, spreadsheets, instrumentation-related and Abbott network systems).<br>
-&nbsp;&nbsp; Produces reports and documents utilizing advanced writing skills.<br>
-&nbsp;&nbsp; Utilizes multiple analytical instruments; trains others in their operation.<br>
-&nbsp;&nbsp; Anticipates, recognizes, and resolves technical problems.</font></font><br>
<br>
LEVEL OF ACCOUNTABILITY:<br>
<strong><font face="Helv" size="1"><font face="Helv" size="1">-&nbsp;&nbsp; Scope: Across programs/within division<br>
-&nbsp;&nbsp; Translates strategic needs of the division into executable programs and projects.&nbsp;<br>
-&nbsp;&nbsp; Responsible for own Redbook documentation, and for the accuracy, quality, and timeliness of experimental results.<br>
-&nbsp;&nbsp; Analyzes data and results from multiple experiments, formulates conclusions, and determines future experiments.<br>
-&nbsp;&nbsp; Actively participates in routine maintenance, lab safety; may assume roles of responsibility, such as training or document control.</font></font><br>
<br>
LEADERSHIP ACTIVITIES:<br>
<strong><font face="Helv" size="1"><font face="Helv" size="1">-&nbsp;&nbsp; Prepares results of projects internally and may present externally.<br>
-&nbsp;&nbsp; Reviews, evaluates, and critiques presentations for others.<br>
-&nbsp;&nbsp; Presents complex technical data to large and diverse groups.<br>
-&nbsp;&nbsp; Trains others on the theoretical and practical basis of advanced techniques, processes, and assays.<br>
-&nbsp;&nbsp; Establishes the project approach. Leads project planning, updates, and process improvements.<br>
-&nbsp;&nbsp; Generates new product ideas consistent with division strategy.<br>
-&nbsp;&nbsp; Prepares and aligns goals with manager's goals.<br>
-&nbsp;&nbsp; Coaches lower-level scientists (e.g., presentation skills, negotiation skills, decision-making, and contingency planning).<br>
-&nbsp;&nbsp; Influences decision-making through negotiation, addressing conflict, and by building productive working relationships across programs/within division.</font></font><br>
<br>
INTERPERSONAL SKILLS:<br>
-&nbsp;&nbsp; P<strong><font face="Helv" size="1"><font face="Helv" size="1">anticipate in technology teams.<br>
-&nbsp;&nbsp; Maintain and develop broad external and internal contacts as required to accomplish job objectives.</font></font><br>
</strong></strong></strong></strong></strong></strong></font></font>

<p><b>QUALIFICATIONS:</b></p>

<p><font size="2">Basic Qualifications:&nbsp;<br>
<strong><font face="Helv" size="1"><font face="Helv" size="1">

<p><strong><font face="Helv" size="1"><font face="Helv" size="1">Knowledge of regulations and standards affecting IVDs and Biologics.</font></font></strong></p>

<p>&nbsp;</p>

</font></font>Position may be graded B6/B7 based on candidate's skills/experience level.<br>
<br>
Preferred Qualifications:</strong></font></p>

<p><font color="#33cc00" size="2">

<p><span style="FONT-FAMILY: Arial"><span style="FONT-FAMILY: Arial"><font color="#0066cc">Through numerous local, national and international accolades, Abbott is regarded as an employer of choice for our commitment to workplace excellence. Our employees are given the tools to succeed, lead and grow, with challenging opportunities and work that makes a difference. Through our diverse healthcare businesses, we connect people and potential in ways that no other company can. </font></span></span></p>

<p><span style="FONT-FAMILY: Arial"><font color="#0066cc">Discover a world of opportunities at Abbott. </font></span></p>

<p><font color="#0066cc"><span style="FONT-FAMILY: Arial">&nbsp;</span><strong style="mso-bidi-font-weight: normal"><span style="FONT-FAMILY: Arial"><em>EEO Statement: </em></span></strong></font></p>

<p><span style="FONT-FAMILY: Arial"><em><font color="#0066cc">At Abbott, we believe that diversity drives innovation. Innovative thinkers who are passionate about the work they do, Abbott employees are representative of the diversity of the patients we strive to serve every single day across the globe.</font></em></span></p>

</font>

<br>
<br>
If interested, please apply online at <a href="http://track.jobviper.com/ViewJob.asp?id=650221-1432-8418"  rel="nofollow">http://track.jobviper.com/ViewJob.asp?id=650221-1432-8418</a>
]]></description>
<dc:date>2009-11-06T08:20:29-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/nsd/sci/1454036030.html</dc:source>
<dc:title><![CDATA[ PRINCIPAL SCIENTIST II (Carlsbad, CA)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-06T08:20:29-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1453318471.html">
<title><![CDATA[Associate Director, Licensing at Gen-Probe (Sorrento Mesa)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1453318471.html</link>
<description><![CDATA[<b>“The Power to Look Deeper”</b><br>
Awarded the 2008 Grand Prize at the local Workplace Excellence Awards, Gen-Probe is a respected biotech employer of choice in San Diego and a global leader in the research, development, manufacturing and marketing of nucleic acid probe-based products used for the diagnosis of human diseases and for screening of donated human blood.  We offer a state-of-the-art facility in a prime location with world-class benefits. We’re currently looking for team members who have “The Power to Look Deeper” in developing the best products, technologies and service.<br>
<br>
<b>“The Power to Shape Your Future”</b><br>
We are seeking an <b>Associate Director, Licensing</b> who will provide expertise in the area of licensing for key strategic planning and business development projects.  This person will be an in-house subject matter expert in the areas of <b>in/out licensing, intellectual property, and technical patents. </b><br>
<br>
<b>DESCRIPTION OF POSITION RESPONSIBILITIES:</b><br>
•Identify, evaluate and analyze new licensing partnerships and opportunities.<br>
•Conduct negotiations related to licensing and other business agreements.<br>
•Manage the preparation and review of licensing agreements.<br>
•Partner with corporate counsel to draft documents, agreements, etc.<br>
•Manage company IP/Patent database.<br>
•Establish and maintain relationships with Gen-Probe licensing partners.<br>
<br>
<b>EDUCATION & EXPERIENCE:</b><br>
•Bachelors Degree (preferably in Sciences) required; MBA strongly preferred.<br>
•8+ yrs licensing, strategic planning, business development experience within the Life Sciences industry required.  Diagnostics industry experience preferred but not required.<br>
•Strong negotiating background <br>
•Must possess strong interpersonal skills to interface effectively with all levels of management. <br>
•25% domestic/international travel required.<br>
<br>
<b>Gen-Probe offers a dynamic and innovative work environment along with excellent benefits that include company sponsored medical/dental/vision benefits, stock options (NASDAQ:GPRO), bonus potential, 401(k) with company match, paid vacation/sick time /holidays, assistance with continuing education, on-site fitness center and our own Waterfall Café.</b>  <br>
<br>
We invite you to view our Career Video!<br>
<b><a href="http://www.view-career-video.com/videos/genprobe/"  rel="nofollow">http://www.view-career-video.com/videos/genprobe/</a></b><br>
<br>
Please apply online by visiting:<br>
<b><a href="http://www.genprobe.com/careers/opportunities.aspx"  rel="nofollow">http://www.genprobe.com/careers/opportunities.aspx</a></b> <br>
]]></description>
<dc:date>2009-11-05T15:58:40-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1453318471.html</dc:source>
<dc:title><![CDATA[Associate Director, Licensing at Gen-Probe (Sorrento Mesa)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-05T15:58:40-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1453314580.html">
<title><![CDATA[Sr. Systems Engineer (Med Device) at Gen-Probe (Sorrento Mesa)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1453314580.html</link>
<description><![CDATA[<b>“The Power to Look Deeper”</b><br>
Awarded the 2008 Grand Prize at the local Workplace Excellence Awards, Gen-Probe is a respected biotech employer of choice in San Diego and a global leader in the research, development, manufacturing and marketing of nucleic acid probe-based products used for the diagnosis of human diseases and for screening of donated human blood.  We offer a state-of-the-art facility in a prime location with world-class benefits.<br>
<br>
<b> “The Power to Shape Your Future”</b><br>
We are seeking an experienced <b>Sr. Systems Engineer</b> to support system integration activities across various engineering projects.  Candidates should have <b>experience with the development and commercialization of complex medical diagnostics instrumentation</b>, including some background with design control methodologies in an FDA QSR environment and expertise in developing technical documentation needed to support regulatory submissions.<br>
 <br>
<b>DESCRIPTION OF POSITION RESPONSIBILITIES:</b><br>
•Plans, develops, and implements system testing programs for complex medical diagnostics instrumentation.<br>
•Leads or provides guidance to help resolve complex technical problems requiring multiple areas of expertise.<br>
•Analyzes test data, manufacturing and field failures and makes recommendations for product and process improvement.<br>
•Leads, designs, execute, and documents system level characterization tests for product feasibility, development, and validation.<br>
•Participates on cross-functional teams to create product and subsystem requirements and to perform product risk analyses.<br>
•May supervise one or more junior personnel<br>
<br>
<b>RELATED BUSINESS/TECHNICAL SKILLS, KNOWLEDGE, ABILITIES:</b><br>
•Demonstrated expertise to provide solutions to management, R&D staff, and core teams for technical strategies, and resolution of product or project problems, improvements, or field complaints.<br>
•Ability to plan and supervise execution of complex projects or multiple less complex projects, keep to timelines and prioritize resources•	<br>
•Excellent skills in experimental design, root-cause analysis and statistical analysis; ability to analyze complex data and come to valid scientific conclusions.<br>
•Leadership skills as a technical leader and technical decision maker in assigned project areas<br>
<br>
<b>EDUCATION AND EXPERIENCE REQUIREMENTS:</b><br>
•BS/MS in Engineering, Bioengineering, or related field with at least 10 years of relevant systems engineering experience, preferably within the Medical Device, or closely related, industry.<br>
•Broad understanding of multiple engineering disciplines (e.g. electrical, mechanical, liquid handling, thermal analysis, software). <br>
<br>
<b>Gen-Probe offers a dynamic and innovative work environment along with excellent benefits that include sponsored medical/dental/vision benefits, stock options (NASDAQ:GPRO), bonus potential, 401(k) w/company match, paid vacation/sick time /holidays, assistance with continuing education, on-site fitness center, and our own Waterfall Café.</b>  <br>
<br>
We invite you to view our Career Video!<br>
<b><a href="http://www.view-career-video.com/videos/genprobe/"  rel="nofollow">http://www.view-career-video.com/videos/genprobe/</a></b><br>
<br>
Please apply online by visiting:<br>
<b><a href="http://www.genprobe.com/careers/opportunities.aspx"  rel="nofollow">http://www.genprobe.com/careers/opportunities.aspx</a></b> <br>
]]></description>
<dc:date>2009-11-05T15:55:44-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1453314580.html</dc:source>
<dc:title><![CDATA[Sr. Systems Engineer (Med Device) at Gen-Probe (Sorrento Mesa)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-05T15:55:44-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/nsd/sci/1453294593.html">
<title><![CDATA[Associate scientist wanted (San Diego)]]></title>
<link>http://sandiego.craigslist.org/nsd/sci/1453294593.html</link>
<description><![CDATA[A chemistry lab based in San Diego has an opening for an Associate Scientist.  Qualified candidates will have a B.S. or M.S. in chemistry with 3-4 years of experience in related industries.   Qualified candidates will be able to perform multistep synthesis of target molecules, scale-up of intermediates and final target, purification using chromatography techniques and crystallization.  ]]></description>
<dc:date>2009-11-05T15:40:44-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/nsd/sci/1453294593.html</dc:source>
<dc:title><![CDATA[Associate scientist wanted (San Diego)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-05T15:40:44-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1452643084.html">
<title><![CDATA[Research Bioengineer]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1452643084.html</link>
<description><![CDATA[SRI International is a world-leading independent research and technology development organization with almost $300 million in annual revenues. SRI performs multidisciplinary, client-sponsored research and development for government agencies, commercial businesses, and private foundations. To help bring its innovations to market, SRI licenses its technologies, fosters strategic partnerships, and creates new companies. Together, SRI and its subsidiary Sarnoff Corporation have spun off about two dozen companies to date.<br>
<br>
Innovations from SRI touch our lives every day. Achievements include the invention of the computer mouse, an important role in the birth of the Internet, and automated check processing for banking.  Drugs discovered and developed by SRI are improving and saving lives around the world. The institute's education research is helping improve teaching and learning. SRI has met mission-critical national defense needs for decades, from the Cold War to today's war against terrorism.<br>
<br>
SRI, a nonprofit corporation, was founded in 1946 as the Stanford Research Institute, and became independent from Stanford University in 1970.<br>
<br>
For additional information, please visit us at <a href="http://www.sri.com"  rel="nofollow">http://www.sri.com</a><br>
<br>
Chemistry, physics, materials science, mechanics, optics, and nanotechnology - these are areas underlying many new applications and market opportunities. SRI International's Physical Sciences Division (www.sri.com/psd) offers government and commercial clients worldwide the diverse technical expertise needed to address important technical challenges in these and many other fields. Our work ranges from fundamental research and laboratory experiments to computer simulations, pilot-scale testing, systems development and commercialization of products.<br>
For additional information, please visit the Physical Sciences Division website: <a href="http://www.sri.com/psd"  rel="nofollow">http://www.sri.com/psd</a><br>
<br>
We have an immediate opening for a Research Bioengineer to work with a multidisciplinary team developing biosensors using novel DNA microarrays.  Will be responsible for performing molecular biology experiments using bacteria, yeasts, viruses and fungi.  Experience with cell separation, cellular sub component extraction (proteins, mRNA, and DNA), purification of cellular products, and PCR amplification required.  Will apply laboratory experience to the development of fieldable sensor systems that are capable of real-time end-to-end processing and detection.  Will also work with laboratory managers developing new sensor systems concepts for a variety of DoD applications.  Should be proficient in various biosensor technologies.<br>
<br>
Requirements:<br>
--BS/MS in Molecular Biology or Bioengineering with six years of hands-on molecular biology experience using a broad range of laboratory techniques.<br>
--Must have a current Top Secret or Q security clearance, or have had an active TS or Q clearance within the last 24 months. <br>
--Proficient in using molecular biology analytical equipment and military biosensor systems.<br>
--Proficient with computers.<br>
<br>
A post-offer, pre-laboratory physical examination will be required.<br>
<br>
How to apply:<br>
Apply via our web page www.sri.com/jobs to job number 100282<br>
SRI is an equal opportunity employer.<br>
www.sri.com/jobs<br>
]]></description>
<dc:date>2009-11-05T09:06:44-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1452643084.html</dc:source>
<dc:title><![CDATA[Research Bioengineer]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-05T09:06:44-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1452429564.html">
<title><![CDATA[Principal Scientist, Cell Biology  (San Diego, CA )]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1452429564.html</link>
<description><![CDATA[Celula, Inc. is a San Diego venture capital backed company developing rare-cell diagnostic systems to address significant unmet medical needs. Celula provides outstanding career opportunities for innovative and motivated team players who are committed to making a difference in science and human healthcare.<br>
<br>
We are searching for an experienced professional to join our growing, dynamic team! <br>
The ideal candidate will have the following areas of expertise: Cell Biology, Biochemistry, Hematopoiesis, Antibody Optimization, Flow Cytometry and Magnetic Cell Selection.<br>
<br>
This scientist will lead a team and interact with a multidisciplinary group of Cell Biology, Biochemistry, and Engineering scientists to develop novel cell enrichment techniques and assays. The hands-on scientist will design, manage and directly execute the enrichment of novel rare-cell populations from blood. Responsibilities will include research, experimental planning, and execution through hands-on experimentation, and direction of a group of research associates. This person will also be responsible for analysis, summary and presentation of data to other scientists and senior management.<br>
<br>
Requirements and Qualifications:<br>
<br>
•	PhD and a minimum of 5 years relevant scientific and project lead experience required. <br>
•	Extensive experience with methods of magnetic-bead based separation and flow- cytometry, including analysis and FACS for the identification and/or isolation of rare cell populations such as hematopoietic lineages, tumor, or stem cells required. <br>
•	Experience with biochemistry of cell labeling and antibody staining required. <br>
•	Experience with antibody selection, conjugation chemistries, and specificity validation required. <br>
•	Familiarity with the current developments in stem cells research in terms of identification, separation, and potential for clinical applications required. <br>
•	Demonstrated ability to successfully complete complex projects with challenging timelines.<br>
•	Developed novel assays or cell enrichments in a product development or clinical setting a plus.<br>
•	Function independently and work on multidisciplinary team-based projects required. <br>
•	Experience with PCR; Q-PCR/Real-time PCR experience a plus.<br>
•	Excellent written and verbal communication skills required. <br>
<br>
<br>
Celula, Inc. offers a competitive compensation and benefits package, including medical, dental, vision, life, long term care, disability, flex spending accounts, 401k and stock options. <br>
Please send resume and cover letter to: hr@celula-inc.com See our website...www.celula-inc.com<br>
<br>
<br>
<br>
<br>
EOE <br>
<br>
<br>
]]></description>
<dc:date>2009-11-05T06:58:30-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1452429564.html</dc:source>
<dc:title><![CDATA[Principal Scientist, Cell Biology  (San Diego, CA )]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-05T06:58:30-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1452124412.html">
<title><![CDATA[Experienced PhD Scientist Seeking to Get Involved w/ Biotech Start-Up (San Diego)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1452124412.html</link>
<description><![CDATA[I recently relocated to San Diego for a great sales position with a large biotechnology company but my ultimate goal is to get involved with a biotechnology <br>
start-up.  I have lots of experience in the laboratory (genomics, proteomics, clinical) and in support/sales (seminars, demos, etc).  Most importantly I'm hard-working,<br>
creative, and highly self-motivated.  I also have experience writing grants and working for other small companies.  I can bring a lot to the table.  <br>
<br>
I'm looking for a very early stage biotechnology start-up or maybe even somebody with an idea looking to start a company and who needs partners.<br>
<br>
I'm not looking for a salary but would obviously want a part of the action in the case things take off in the future.  I could dedicate 10 +/- hours<br>
per week toward building the business depending on my travel schedule.  Do you have an idea?  Lets talk!]]></description>
<dc:date>2009-11-04T20:18:03-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1452124412.html</dc:source>
<dc:title><![CDATA[Experienced PhD Scientist Seeking to Get Involved w/ Biotech Start-Up (San Diego)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-04T20:18:03-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/ssd/sci/1451824919.html">
<title><![CDATA[Now hiring Multiple Research Associates! (Mira Mesa)]]></title>
<link>http://sandiego.craigslist.org/ssd/sci/1451824919.html</link>
<description><![CDATA[Dear Research Associates,<br>
<br>
A premier biotech company in Mira Mesa is searching for 3 Research Associates to join their team for 3-6+ months. Please submit your resume and references as a word document if you are interested in applying. <br>
<br>
Research Associate I<br>
Duration: 3-6+ months (May be extended) <br>
Pay: $15-17/hr, DOE <br>
<br>
Description:  Support new product integration.  Will be working 80% in the lab. Lab duties include accurate pipetting, handling clinical samples, lab notebook, analyzing and graphing data, using computer tools such as excel, word. Familiarity with diagnostic assays, instrumentation and/or software a plus. Must work in a team environment. Flexibility with work hours also required as team coverage includes evenings and weekend work. <br>
<br>
Requirements: B.S. in the Sciences or Bioengineering and 1-2 years of lab experience.   Strong pipetting skills.  Proficiency for MS Office.]]></description>
<dc:date>2009-11-04T15:56:27-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/ssd/sci/1451824919.html</dc:source>
<dc:title><![CDATA[Now hiring Multiple Research Associates! (Mira Mesa)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-04T15:56:27-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1451618606.html">
<title><![CDATA[Manufacturing Technician (La Jolla)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1451618606.html</link>
<description><![CDATA[Advanced BioHealing (ABH) is a specialty biotechnology company focused on the development and marketing of cell-based and tissue-engineered products. We are a privately held company with two approved products: Dermagraft® and TransCyte®. Our development pipeline also includes a next-generation bioengineered wound therapy for which two Investigational Device Exemption (IDE) applications have been approved by the Food and Drug Administration (FDA).
<br>
We currently have an opening for a Manufacturing Technician at our La Jolla, CA manufacturing facility.
<br>

<br>

<br>
Advanced BioHealing, Inc.
<br>
Position Description
<br>
 
<br>
Job Title: 	Manufacturing Technician
<br>
Department: 	Manufacturing 
<br>

<br>

<br>
The Manufacturing Technician provides support for preparing and sterilizing intermediate products and manufactures final product for commercial distribution. Responsible for following approved procedures (SOPs) and performing daily tasks in a cleanroom per the current QSRs.  Follows established company rules, regulations and safety precautions, and maintains quality standards.  Ensures that high standards of Quality and Teamwork are adhered to.  
<br>

<br>

<br>
ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.
<br>

<br>
•	Responsible for supporting the manufacturing groups.  Duties include maintenance of inventory, ordering supplies, stocking the facility with necessary raw materials by inventory assessment, maintaining minimum inventory requirements, initiating move orders, sanitization of all incoming supplies and transferring of them into the DGM facility; preparation of items for autoclaving , autoclaving,  cleaning and assembly of reusable in-process supply items; supports manufacturing activities with the assembly of sub-assemblies, operation of Manufacturing equipment as necessary.   Preparation of the Quality Control monitoring plates; preparation of labels and general cleanliness of working area; packaging operations.  May require working weekends or shift work.  	
<br>
•	Various other duties that are required to produce product.  Some of these duties may include: cell expansion; cell feeding, harvesting, counting and freezing; product seeding; growth system maintenance; labeling, packaging and freezing of product; and culture media preparation.  In order to perform these duties, Manufacturing Associates must be familiar with paperwork for each task, cleaning procedures, aseptic processing techniques, Good Manufacturing Practices (GMP) and laboratory safety practices and procedures
<br>
•	Performs Production Related tasks as assigned by the area Supervisor or Group Lead.
<br>

<br>

<br>
QUALIFICATIONS  
<br>

<br>
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
<br>

<br>
EDUCATION and/or EXPERIENCE 
<br>

<br>
High school diploma or equivalent; some college education in a life science or related area preferred.  B.S. or related degree not required, but helpful.  Laboratory experience is a plus.   Has knowledge of commonly used production concepts, practices, and procedures.  General knowledge of cleanroom practices, familiarity with Good Manufacturing Practices (GMP).
<br>
	
<br>
LANGUAGE SKILLS 
<br>

<br>
Ability to read, and interpret SOPs and Batch records written in English.  Ability to document activities clearly and neatly.
<br>

<br>
MATHEMATICAL SKILLS 
<br>

<br>
Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals.  Ability to add and subtract two digit numbers and to multiply and divide with 10's and 100's.  Ability to perform these operations using weight measurement, volume, and distance
<br>

<br>
REASONING ABILITY 
<br>

<br>
Ability to apply common sense understanding to carry out detailed but uninvolved written or oral instructions.  
<br>

<br>
PHYSICAL DEMANDS  The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
<br>

<br>
Working in a cleanroom environment required.  Must clothe in cleanroom gowns to perform duties.  Must be able to lift/push 50 lbs.  Many manipulations performed which require good eye/hand coordination. Must have good seeing ability in order to inspect culture, assemblies and packaging.  Must have good talking and hearing abilities in order to interact with team.  Must work with living human cells and various chemicals. Generally, chemicals used are not toxic or extremely dangerous.  However, precautions must be taken with all chemicals, solutions and cultures. Due to the nature of Production work overtime and weekend work is a requirement of employment though it may vary depending on the season and production needs of the company.
<br>

<br>
Please review our website at www.advancedbiohealing.com for more company information.
<br>
We offer a competitive benefits & compensation package!
<br>
All qualified resumes should be submitted directly to careers@advancedbiohealing.com
<br>

<br>
We are an Equal Opportunity Employer.
<br>
]]></description>
<dc:date>2009-11-04T13:36:25-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1451618606.html</dc:source>
<dc:title><![CDATA[Manufacturing Technician (La Jolla)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-04T13:36:25-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1451455076.html">
<title><![CDATA[Packaging/Lab Technician (Mira Mesa)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1451455076.html</link>
<description><![CDATA[Leading biotech company in Mira Mesa has an immediate openings for an experience Packaging/Lab Technicians. The successful candidate will have 1+ years recent experience packaging at a biotech or life sciences company. This position will subdivide, label and package biochemicals using defined procedures. This includes, weighing powder and liquid material, utilizing electronic balances/scales and pipettes.  Fills appropriate containers with correct quantity and seals, labels and packages final product. <br>
Materials required may include solvents, measuring equipment, safety clothing equipment, bulk powder and liquids. Experience with SAP is a plus, along with experience in writing or revising SOPs and work instructions. Must be able to stand for extended periods and lift or move up to 50 pounds unassisted. <br>
Must have experience using: <br>
-the metric system sufficient to perform basic math calculations. <br>
-the use of electronic scales, including analytical and micro-balances, pipettes, graduated cylinders. <br>
-and solid experience in the use of computer and MS Office applications. <br>
Basic Knowledge of ISO9000 or Good Manufacturing Practices(GMP)<br>
Hours are M-F 6am -2:30 pm. Qualified candidates please submit your resume via e-mail for immediate consideration.]]></description>
<dc:date>2009-11-04T11:59:45-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1451455076.html</dc:source>
<dc:title><![CDATA[Packaging/Lab Technician (Mira Mesa)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-04T11:59:45-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1450304423.html">
<title><![CDATA[Quality Control Associate I (San Diego)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1450304423.html</link>
<description><![CDATA[Our History of Expertise & Quality Focus<br>
<br>
Established in 1999, eBioscience, Inc. is a rapidly growing, fast-paced biotech company providing innovative high quality reagents to researchers worldwide that empower the process of scientific discovery in the areas of cellular immunity and oncology. Our extensive portfolio of leading edge cell analysis products and technologies, focused on flow cytometry and immunodetection, position our customers to be at the forefront of science. Product line applications include reagents for multi-color flow and immunofluorescence, bioassays, ELISA, ELISPOT and western blot. We are committed to developing and producing a large selection of innovative and commonly used reagents at high quality and great prices. We offer unique opportunities for talented and motivated individuals to gain company ownership and rapid career advancements.<br>
<br>
Quality Control Associate<br>
<br>
We are seeking a highly motivated Quality Control Associate accountable for in-process testing of bulk materials, and finished products. Responsibilities include performing a wide variety of laboratory tasks within a team environment. Specifically, running, and trouble-shooting Flow Cytometry, ELISA, Bioassay, and western Blot assays to assist in the quality testing of innovative antibody-based assays. In addition, this individual will adhere to all requirements of established quality systems.<br>
<br>
Essential Duties and Responsibilities (other duties may be assigned.):<br>
<br>
•	Conduct in-process and final product testing following Standard Operating Procedures<br>
•	Responsible for assuring that products are tested to meet the highest quality standards as determined by performance specifications.<br>
•	Responsible for ensuring that QC tasks are completed according to: schedule, company policies, procedures and test methods.<br>
•	Effectively implement and maintain the company's standard operating procedures for Quality Control. <br>
•	Understands test results and pursues clarification of unusual results. Develops and uses system for anticipating and recognizing errors. Resolves discrepancies and reports results.<br>
•	Adheres to good documentation practices to ensure data integrity and traceability.<br>
<br>
Qualifications:<br>
<br>
The position requires a Bachelor's degree in Biology or a closely related field with relevant experience with 0-2 years of work experience in a Research or GMP Quality Control laboratory. Current experience performing a variety of antibody based assays for bulk materials, in-process materials and finished products is highly preferred. Experience writing and modifying Standard Operating Procedures is preferred. Fundamental knowledge of regulatory requirements, such as current GMP regulations and the ability to review and understand test data is highly desirable. Understanding and the ability to follow safety precautions and procedures which apply to the activities in the laboratory is required. Strong attention to detail and ability to work in a dynamic fast paced environment is a necessity. Must be able to collaborate across multidisciplinary teams and also have the ability to work independently. Candidate must have strong math skills; strong scientific background; excellent skills in prioritization and achievement of goals and objectives. Excellent written and verbal communication skills, a strong work ethic, computer literacy, and the ability to work independently following verbal instructions and SOPs are required. Flexibility and a passion to drive for results are key for this position.<br>
<br>
Physical Demands and Work Environment:<br>
<br>
The physical demands and work environment described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.<br>
While performing the duties of this job, the employee is regularly required to sit, stand, walk, talk and hear; use hands to finger, handle or feel; and reach with hands and arms. The employees will occasionally be exposed to hazardous materials in small amounts.  Close vision, color vision, and ability to adjust focus are required.<br>
<br>
The noise level in the environment is usually moderate.<br>
<br>
Benefits:<br>
<br>
We offer an exciting, entrepreneurial environment and a competitive compensation package, including salary, plus performance bonus and benefits (medical/dental and 401k). Plus, we work to maintain the best possible environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where each person feels encouraged to contribute to our processes, decisions, planning and culture. Our company culture is creative, fast-paced and entrepreneurial. We are a right sized environment where you can stand out and make a difference.<br>
<br>
To Apply<br>
<br>
Please submit resume with salary history and requirements to careers@ebioscience.com, referencing Quality Control Associate in the Subject Line.<br>
<br>
EOE<br>
<br>
]]></description>
<dc:date>2009-11-03T15:56:14-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1450304423.html</dc:source>
<dc:title><![CDATA[Quality Control Associate I (San Diego)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-03T15:56:14-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/nsd/sci/1450248054.html">
<title><![CDATA[Postdoctoral Fellow (392) (La Jolla, CA)]]></title>
<link>http://sandiego.craigslist.org/nsd/sci/1450248054.html</link>
<description><![CDATA[Postdoctoral Fellow-Division of Inflammation Biology <br>
<br>
Please apply directly to: careers.liai.org/applicants/Central?quickFind=50331   <br>
<br>
La Jolla Institute for Allergy & Immunology (www.liai.org)<br>
<br>
Our independent, non-profit research group is currently seeking several highly motivated postdoctoral researchers for positions in the laboratory of Dr. Joel Linden. The research focus of the laboratory is the regulation of the NK and T cell anergy. Ideal postdoctoral candidates will have a strong background in purinergic signaling, type II diabetes, cancer immunology, sickle cell anemia or immune cell signaling  with no more than two years of prior postdoctoral experience. Position is available beginning in January 2010. Interested individuals should send their curriculum vitae, a cover letter or research statement listing prior research experience and current research interests, and the names of three references.<br>
<br>
Please apply directly to: careers.liai.org/applicants/Central?quickFind=50331   ]]></description>
<dc:date>2009-11-03T15:15:40-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/nsd/sci/1450248054.html</dc:source>
<dc:title><![CDATA[Postdoctoral Fellow (392) (La Jolla, CA)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-03T15:15:40-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1450006448.html">
<title><![CDATA[Molecular Biologist (Mira Mesa)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1450006448.html</link>
<description><![CDATA[Leading Mira Mesa biotech company  has an immediate need for an experienced Molecular Biologist. Will make products (RNA/DNA markers, vectors, phage...) solely based on protocol. Qualified candidate will have a minimum of 10 years relevant experience. This is a contract position through the end of the year requiring mandatory overtime. Please submit your resume for immediate consideration. <br>
 ]]></description>
<dc:date>2009-11-03T12:42:14-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1450006448.html</dc:source>
<dc:title><![CDATA[Molecular Biologist (Mira Mesa)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-03T12:42:14-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1449818976.html">
<title><![CDATA[Salk Institute for Biological Studies- C235 Research Assistant I (La Jolla, CA)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1449818976.html</link>
<description><![CDATA[The Salk Institute for Biological Studies is currently seeking a Research Assistant I for our Viral Vector Core Facility. The facility focuses on providing custom viral vectors supporting the work of participating scientists. Department produces research-level viral vectors, including lentivirus and adeno-associated virus (AAV).
<p>
Research and lab responsibilities will include:
<ul>
<li>Production and purification of viral vectors as a service to internal and external investigators.</li>
<li>Work with biohazardous agents under Biosafety level II+ conditions.</li>
<li>Perform standard molecular biology techniques including plasmid construction and propagation, DNA/RNA isolation and purification, cloning, PCR and QPCR, etc.</li>
<li>Routine cell culture and maintenance of cell lines and cell stocks.</li>
<li>Troubleshoot and modify protocols to obtain optimal results.</li>
<li>Assist in general lab maintenance; including preparation of reagent and buffer stocks, maintenance of equipment and databases, preparation and testing of new protocols and ordering of supplies.</li>
</ul>
<p>
Education: Bachelor's degree in life sciences (biology, microbiology, biochemistry, etc.).
<p>
Experience: 1-2 years of research lab experience. Hands-on experience with cloning, plasmid construction and molecular biology is essential. Experience with routine tissue culture is desirable. Computer literate and proficient with Microsoft Office, especially Excel is required. Proven ability to work with minimal supervision is also required.
<p>
Special Requirements: Seeking a reliable, self-motivated individual. Attention to detail and the ability to maintain accurate records is especially important. Previous experience working in BSL2 lab and/or experience with viral vector production is preferred.
<p>
Position is available immediately. Flexible work schedule can be negotiated. Some overtime and weekend work is expected.
<p>
<center><b>Interested applicants should submit a cover letter detailing previous research experience and professional references with a resume by November 16, 2009 to <a href="http://salk.edu/careers/staff_positions.html"  rel="nofollow">http://salk.edu/careers/staff_positions.html</a></center></b>]]></description>
<dc:date>2009-11-03T10:57:31-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1449818976.html</dc:source>
<dc:title><![CDATA[Salk Institute for Biological Studies- C235 Research Assistant I (La Jolla, CA)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-03T10:57:31-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/nsd/sci/1449436561.html">
<title><![CDATA[SR. SCIENTIST LV III (Carlsbad, CA)]]></title>
<link>http://sandiego.craigslist.org/nsd/sci/1449436561.html</link>
<description><![CDATA[<p><font size="2">

<p><span style="FONT-FAMILY: Arial"><font color="#33cc33"><font color="#0066cc">At Abbott, we provide the perspectives and experience necessary to translate science into real solutions for patients in over 130 markets worldwide. Today, 72,000 Abbott employees are doing work that matters.</font></font></span></p>

</font></p>

<p><font size="1"><strong>PRIMARY FUNCTION:<br>
</strong></font><font face="Helv"><font face="Helv" size="1"><strong>-&nbsp;&nbsp; Conceives, plans, designs, and conducts advanced independent research.<br>
<font face="Arial">-&nbsp;&nbsp;&nbsp;Investigates</font> and develops new procedures.&nbsp;<br>
-&nbsp;&nbsp; Direction provided by project goals and experimental design.<br>
-&nbsp;&nbsp; May act as project leader, lead scientist, or independent reviewer.&nbsp;<br>
-&nbsp;&nbsp; Provides technical direction and feedback to others.<br>
-&nbsp;&nbsp; Interacts with other groups and shares information; participates in team activities.<br>
<br>
EXPERTISE AND PROBLEM-SOLVING RESPONSIBILITIES:<br>
-&nbsp;&nbsp; Responsible for implementing and maintaining the effectiveness of the quality system.<br>
-&nbsp;&nbsp; Understands and consistently follows documented procedures.<br>
-&nbsp;&nbsp; Determines priorities for experiments.<br>
-&nbsp;&nbsp; Applies quantitative methods: analyzes data, evaluates results, forms conclusions, and provides/implements process or document improvements.<br>
-&nbsp;&nbsp; Independently designs and executes a series of experiments to test hypotheses related to project outcomes.<br>
-&nbsp;&nbsp; Applies advance scientific knowledge to projects.<br>
-&nbsp;&nbsp; Utilizes DOE where appropriate.<br>
-&nbsp;&nbsp; May assist in the design of experiments for others.<br>
-&nbsp;&nbsp; Identifies technical alternatives from literature review.<br>
-&nbsp;&nbsp; Applies basic computer skills (includes word processing, spreadsheets, instrumentation-related and Abbott network systems).<br>
-&nbsp;&nbsp; Produces reports and documents utilizing advanced writing skills.<br>
-&nbsp;&nbsp; Utilizes multiple analytical instruments; trains others in their operation.<br>
-&nbsp;&nbsp; Recognizes and resolves technical problems.<br>
<br>
LEVEL OF ACCOUNTABILITY:<br>
-&nbsp;&nbsp; Scope: Across functional areas<br>
-&nbsp;&nbsp; Defines project goals and is responsible for timely project completion.<br>
-&nbsp;&nbsp; Responsible for own Redbook documentation, and for the accuracy, quality, and timeliness of experimental results.<br>
-&nbsp;&nbsp; Summarizes data and analyzes results, independently formulates conclusions, and determines future experiments.<br>
-&nbsp;&nbsp; Actively participates in routine maintenance, lab safety; may assume roles of responsibility, such as training or document control.<br>
<br>
LEADERSHIP ACTIVITIES:<br>
-&nbsp;&nbsp; Prepares results of projects internally and may present externally.<br>
-&nbsp;&nbsp; Reviews, evaluates, and critiques presentations for others.<br>
-&nbsp;&nbsp; Presents complex technical data to large and diverse groups.<br>
-&nbsp;&nbsp; Trains others on the theoretical and practical basis of techniques, processes, and assays.<br>
-&nbsp;&nbsp; Participates in project planning, updates, and process improvements.<br>
-&nbsp;&nbsp; May generate new product ideas consistent with division strategy.<br>
-&nbsp;&nbsp; Prepares and aligns goals with manager's goals.<br>
-&nbsp;&nbsp; May coach lower-level scientists (e.g., presentation skills, negotiation skills, decision-making, and contingency planning).<br>
-&nbsp;&nbsp; Influences decision-making through negotiation, addressing conflict, and by building (productive) working relationships across functional areas.<br>
<br>
INTERPERSONAL SKILLS:<br>
-&nbsp;&nbsp; Participate in technology teams.<br>
-&nbsp;&nbsp; Develop and maintain internal and external customer contacts to maintain technical knowledge as required to accomplish objectives.</strong></font></font>

<p><b>QUALIFICATIONS:</b></p>

<p><font size="2">Basic Qualifications:&nbsp;<br>
<strong><font face="Helv" size="1"><font face="Helv" size="1">

<p>Knowledge of regulations and standards affecting IVDs and Biologics.</p>

</font></font>Position may be graded B5/B6 based on candidate's skills/experience level.<br>
<br>
Preferred Qualifications:</strong></font></p>

<p><font color="#33cc00" size="2">

<p><span style="FONT-FAMILY: Arial"><span style="FONT-FAMILY: Arial"><font color="#0066cc">Through numerous local, national and international accolades, Abbott is regarded as an employer of choice for our commitment to workplace excellence. Our employees are given the tools to succeed, lead and grow, with challenging opportunities and work that makes a difference. Through our diverse healthcare businesses, we connect people and potential in ways that no other company can. </font></span></span></p>

<p><span style="FONT-FAMILY: Arial"><font color="#0066cc">Discover a world of opportunities at Abbott. </font></span></p>

<p><font color="#0066cc"><span style="FONT-FAMILY: Arial">&nbsp;</span><strong style="mso-bidi-font-weight: normal"><span style="FONT-FAMILY: Arial"><em>EEO Statement: </em></span></strong></font></p>

<p><span style="FONT-FAMILY: Arial"><em><font color="#0066cc">At Abbott, we believe that diversity drives innovation. Innovative thinkers who are passionate about the work they do, Abbott employees are representative of the diversity of the patients we strive to serve every single day across the globe.</font></em></span></p>

</font>

<br>
<br>
If interested, please apply online at <a href="http://track.jobviper.com/ViewJob.asp?id=649594-1432-6318"  rel="nofollow">http://track.jobviper.com/ViewJob.asp?id=649594-1432-6318</a>]]></description>
<dc:date>2009-11-03T07:27:18-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/nsd/sci/1449436561.html</dc:source>
<dc:title><![CDATA[SR. SCIENTIST LV III (Carlsbad, CA)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-03T07:27:18-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1448895095.html">
<title><![CDATA[Manufacturing Quality Systems Specialist / Auditor (Sorrento - Mesa)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1448895095.html</link>
<description><![CDATA[Cyntellect, a small biotech company in Sorrento-Mesa, has an immediate need for a Manufacturing Quality Systems Specialist / Auditor.  This is a one month, temporary assignment. This person would need a proven background in:<br>
<br>
1.	Conducting manufacturing audit per TuV factory performance requirements <br>
2.	Hands-on quality system changes to bring us in conformity with the above audit results and recommending internal QC checks for product quality.<br>
3.                  Experience required in CE/TuV product and manufacturing approval<br>
<br>
Please include your salary requirements with your resume. ]]></description>
<dc:date>2009-11-02T17:36:59-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1448895095.html</dc:source>
<dc:title><![CDATA[Manufacturing Quality Systems Specialist / Auditor (Sorrento - Mesa)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-02T17:36:59-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1448824841.html">
<title><![CDATA[Research Associates (6 month temp)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1448824841.html</link>
<description><![CDATA[BioPhase Solutions specializes in recruiting top talented professionals for San Diego's Scientific community. We are currently looking for Research Associates to work for a leading San Diego biotechnology company.<br>
<br>
Research Associates<br>
<br>
Assists with the development of diagnostic assays and analytical methods for the transfer of technology to the Clinical Laboratory in an interdisciplinary R&D department.<br>
<br>
ESSENTIAL DUTIES AND RESPONSIBILITIES <br>
<br>
-Performs experimental procedures from written SOP's <br>
-Assists in the development of new assays <br>
-Contributes to the improvement of existing assays and in the development of new tests <br>
-Assists in the analysis of data utilizing Microsoft Access, Excel and other graphing programs<br>
-Maintains databases as needed <br>
-Performs experiments utilizing molecular biology procedures such as nucleic acid extraction, PCR, RT-PCR, and hybridization assays <br>
-Performs experiments utilizing immunological procedures such as immunostaining, immunoassay and Western Blot techniques <br>
-Assists with assay transfer to the Clinical Laboratory<br>
<br>
EDUCATION and/or EXPERIENCE <br>
<br>
Position generally requires a bachelor's degree (B.A./B.S.) in the biological sciences from four-year college or university; with 0-2 years research and/or laboratory experience in molecular biology and/or immunochemistry experience. Experience in working in GLP/FDA/CLIA regulated atmosphere preferred.<br>
<br>
Please also visit www.biophaseinc.com to view additional opportunities in San Diego County!<br>
]]></description>
<dc:date>2009-11-02T16:45:04-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1448824841.html</dc:source>
<dc:title><![CDATA[Research Associates (6 month temp)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-02T16:45:04-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/nsd/sci/1448516497.html">
<title><![CDATA[Director, Regulatory Affiars (Carlsbad, CA)]]></title>
<link>http://sandiego.craigslist.org/nsd/sci/1448516497.html</link>
<description><![CDATA[Fantastic medical device company in North County San Diego is currently recruiting for a Director of Regulatory Affairs.  Position will report to CEO.  This is a terrific opportunity for someone with 10 years in the medical device industry and 5 years managing the regulatory function and submitting 510(k)'s.  Position is somewhat person-dependent, and could also be a VP level over Regulatory Affairs and Clinical Affairs.
<br>

<br>
Major Responsibilities:
<br>
Scope: Receives assignments in the form of objectives and establishes goals to reach objectives.  Objectives are reviewed by Senior Management to determine success of the position.  Involved in developing, modifying and executing company policies that affect regulatory issues and may have a company-wide effect.
<br>
Job Complexity: Works on complex problems in which analysis of situations requires an in-depth evaluation of various factors.  Exercises judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions.  Acts as advisor to colleagues to meet schedules and/or solve problems.  Develops and administers budgets, schedules and performance requirements.
<br>
Discretion: Erroneous decisions will result in critical delays in schedules and operations and may jeopardize overall business activities.
<br>
Interaction: Regularly interfaces with senior management on matters concerning overall company issues.  Routinely interfaces with external regulatory entities concerning regulatory status and submissions.  Works directly with regulatory consultants, legal counsel, Notified Bodies, Authorized Representatives, FDB and FDA.  Requires the ability to change thinking or gain acceptance of others in sensitive situations.
<br>
Supervision: Manages through other departments to achieve work requirements.  This is a functional manager and may not have subordinates.
<br>
Behavior:  Must exhibit Company values, practice professional and intellectual integrity, exhibit ethical behaviors and be respectful to others at all times.  Must be professional in demeanor and image, deal with differences constructively and be willing to stand up for convictions.
<br>

<br>
Specific Responsibilities: 
<br>
1.	Provide regulatory support and guidance to project teams and senior management.  
<br>
2.	Prepare and submit FDA and European submissions for approval.  
<br>
3.	Manage process from development of regulatory strategy through to approval.  
<br>
4.	Conduct internal regulatory audits and ensure compliance with all U.S. and international regulatory requirements pertaining to product approval.
<br>
5.	Maintain relationships and act as liaison with Authorized Representatives, FDA reviewers, Notified Bodies, external regulatory legal counsel and regulatory consultants.
<br>
6.	Review complaints and lead vigilance and MDR reporting efforts.
<br>
7.	Review and advise on promotion and advertising materials, labeling, product claims, training materials, publications, press releases or marketing programs to ensure compliance with regulations.  
<br>

<br>
Minimum Requirements – Education, Skills, Experience
<br>
1.	Minimum BA/BS or equivalent in the Life Sciences, Engineering or related area
<br>
2.	Must have a complete mastery in the area of responsibility, including relevant standards, practices, and regulations.  
<br>
3.	Must be able to represent own area well, while taking positions and actions based upon a broad view of the company.
<br>
4.	Must be able to work independently and hands on in a timeline driven startup environment.
<br>
5.	Must have excellent written and oral communication skills.  Requires the ability to write reports and business correspondence.
<br>
6.	Working knowledge of PC applications such as MS Word, Excel, Project and PowerPoint.
<br>
7.	5 years medical device regulatory management experience
<br>
8.	10 years medical device or pharmaceutical regulatory affairs experience
<br>
9.	Must have successfully lead effort to file and receive clearance for a medical device 510(k).  Experience with a 510(k) involving clinical trials is a major advantage.  Experience in gaining CE Marking is helpful
<br>
]]></description>
<dc:date>2009-11-02T13:26:50-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/nsd/sci/1448516497.html</dc:source>
<dc:title><![CDATA[Director, Regulatory Affiars (Carlsbad, CA)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-02T13:26:50-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1447290270.html">
<title><![CDATA[Technology and Patent Literature Research]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1447290270.html</link>
<description><![CDATA[Immediate, Part-time, full-time, virtual: Earn potential rewards for scientific technical documents and develop valuable experience in the exciting field of patent literature research.
<br>

<br>

<br>
Article One Partners (www.articleonepartners.com) lists requests for articles, patents, research papers, product literature or any written information from anywhere in the world that describes particular technologies as of a historic date.   Article One’s research projects are called Patent Studies.
<br>

<br>

<br>
There are over 20 studies listed for some of the most important technologies worldwide, such as pharmaceuticals (Lunesta, Levitra, Geodon etc.), telephone apparati (Speech Processing by RIMM), software (Twitter.com), wireless technology, and Blu-ray disc drives on the Playstation 3.   
<br>

<br>

<br>
Article One Partners needs you to find documented information-- prior art. By searching for prior art, you gain the invaluable experience of researching scientific documents, earn profit-sharing points, and may earn up to $50,000 per study. More than twenty studies are currently offered for over $1,000,000 in compensation rewards. Rewards are distributed when Article One determines that the public written information you submit can show a patent to be invalid. 
<br>

<br>

<br>
Begin work immediately, register at www.articleonepartners.com, browse the Studies (check your eligibility), and apply your knowledge, research and network to find Prior Art.  Article One will review your submissions and tell you if you have earned the cash rewards. Your active participation in Article One will earn profit sharing points. (The profit-sharing plan is described in detail on our website.)
<br>

<br>

<br>
By joining and participating in the community, you earn profit-sharing points.  To learn more, come visit us at articleonepartners.com and register for free as an advisor. Also, Article One Partners will soon be adding new studies soon, so by registering now, advisors can get a head start on submitting new prior art.
<br>

<br>

<br>
Article One Partners is a web-based patent research company that searches for prior art. Prior art refers to the entire body of publicly available information that can potentially invalidate a patent by showing that its ideas were known by the date of invention of the patent. Invalidating prior art shows that an invention described in the claims of a patent existed before a date of invention.  Prior art can also be used to establish the strength of a patent.
<br>

<br>

<br>
The Studies list patents with a description of the technology and the historic date.  Patents are granted because the U.S. Patent Office concludes that the description of the technology in the patent is the first in the world.  But the Patent Office is limited in being able to research worldwide public information.  Article One offers a citizen’s review to check whether the patent description is the first.  If you show an earlier description, you can earn $50k and high profile press as a state of the art researcher for recognition in industry and career building.  
<br>

<br>

<br>
The public written information is called Prior Art.  The historic date by which the Prior Art must be dated is called “Latest Date for Prior Art.”  Each Study links to a patent or patents, and provides a written description of the technology and the latest date for Prior Art.  
<br>

<br>

<br>
- Reduce the monopoly pricing you pay for products covered by patents which should not have been granted, help to reform U.S. patent law – and get compensated for your efforts and the value of your knowledge!
<br>

<br>

<br>
****When you register at AOP, please use the registration code Craig.****]]></description>
<dc:date>2009-11-01T16:49:01-08:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1447290270.html</dc:source>
<dc:title><![CDATA[Technology and Patent Literature Research]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-11-01T16:49:01-08:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1444856586.html">
<title><![CDATA[Research Associates/SRA’s 2004-9PR (La Jolla)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1444856586.html</link>
<description><![CDATA[Synthetic Genomics<br>
<br>
Synthetic Genomics is seeking Research and Sr. Research Associates to join our team in the areas of Gene Discovery and Characterization, Strain Isolation and Improvement, and Production System Development to assist in research involving the identification of novel genes, the development of superior strains of photosynthetic microbes, and the optimization of processes for the production of fuels and chemicals.<br>
<br>
We are seeking individuals possessing knowledge, experience, and skills in one or more of the following categories:<br>
<br>
• Molecular Biology (including DNA isolation, PCR, gene cloning, vector construction, and gene expression analysis)<br>
• Biochemistry (including enzyme assays and characterization)<br>
• Microbiology (including microbial strain isolation and characterization, FACS operation, and/or sequence-based taxonomic identification)<br>
• Bioengineering (including optimization of microbial production and product recovery systems)<br>
• Experience working with photosynthetic microbes is highly desired<br>
• Requires a BS in Molecular Biology, Biochemistry, Microbiology, Plant Biology, Biology or related field and a minimum of 1-5 years relevant experience<br>
<br>
Please submit resume to hr@syntheticgenomics.com or our website at www.syntheticgenomics.com and go to the careers tab.<br>
]]></description>
<dc:date>2009-10-30T15:04:36-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1444856586.html</dc:source>
<dc:title><![CDATA[Research Associates/SRA’s 2004-9PR (La Jolla)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-30T15:04:36-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1444837262.html">
<title><![CDATA[Packaging Lab Technician (Sorrento Valley)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1444837262.html</link>
<description><![CDATA[This position will be responsible to fill, label and bag vials of antibody solutions.  Will also enter label info and generate vial labels.  Be able to use of pipette, scale and other packaging equipment as required.  Other duties include completing batch records, and entering and processing packaging data into database.  May also write SOPs for new packaging procedures and review and edit existing SOPs to reflect changes in procedures.  
<br>

<br>
The position requires a minimum of college coursework in Biology, Bioengineering, Biochemistry, Immunology or related studies.  Minimum 1 year of relevant experience in a laboratory and/or biotech manufacturing and/or filling/bottling/packaging working environment required, including pipetting and use of sterile technique.  Must able to work in fast environment.  Good organizational skills with ability to prioritize task.  Must be self-motivated and dependable, and able to work with minimal supervision and pay close attention to details.  Good verbal and written communication skills.  Must have the ability and knowledge to perform math calculations and measurement conversions.  Must be able to lift 30-40 lbs. unassisted.  
<br>

<br>
<b> All qualified candidates must apply and submit resume online on the Careers page of our website: www.biolegend.com </b>]]></description>
<dc:date>2009-10-30T14:50:38-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1444837262.html</dc:source>
<dc:title><![CDATA[Packaging Lab Technician (Sorrento Valley)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-30T14:50:38-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1444831068.html">
<title><![CDATA[Sr. Research Associate 2004-26PR (La Jolla, CA)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1444831068.html</link>
<description><![CDATA[Synthetic Genomics, Inc<br>
<br>
Sr. Research Associate 2004-26PR<br>
<br>
Position Summary:<br>
Synthetic Genomics is seeking Sr. Research Associates join our team in the areas of Gene Discovery and Characterization, Strain Isolation and Improvement, and Production System Development to assist in research involving the identification of novel genes, the development of superior strains of photosynthetic microbes, and the optimization of processes for the production of fuels and chemicals.<br>
<br>
Essential Duties and Responsibilities:<br>
•	High throughput enzymatic assays<br>
•	Immunoaffinity procedures: Western blots and ELISA<br>
•	Electrophoretic techniques: Agarose, SDS-PAGE (different buffer systems), Urea PAGE, Native gels etc<br>
•	Analytical techniques: HPLC, GC etc<br>
•	Knowledge of Lipid biochemistry and experience with handling photosynthetic microbes is desired<br>
<br>
Qualifications<br>
•	Requires a Masters in Biochemistry, Molecular Biology or a related field with a minimum of 2-5 years of experience in industry or an academic lab<br>
•	Requires experience with enzyme kinetics and assay development<br>
•	Requires experience with various spectroscopic techniques: UV-Visual, Fluorescence etc<br>
•	Requires knowledge and experience with various chromatographic procedures: Affinity, Ion exchange, Hydrophobic, Reverse Phase etc<br>
•	Experience with protein purification procedures<br>
•	Experience with gene cloning and expression of recombinant proteins<br>
<br>
Please submit resume to hr@syntheticgenomics.com or go to our website at www.syntheticgenomics.com and click on careers to view job listings]]></description>
<dc:date>2009-10-30T14:46:07-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1444831068.html</dc:source>
<dc:title><![CDATA[Sr. Research Associate 2004-26PR (La Jolla, CA)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-30T14:46:07-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1443582226.html">
<title><![CDATA[System Integration Engineer (Contract: 20 hours per week)  (San Diego)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1443582226.html</link>
<description><![CDATA[Celula, Inc., a growing San Diego venture backed company, develops innovative instruments for clinical diagnostics and biomedical research using advanced micro-fluidics and other technologies. Celula identifies, develops, and validates unique cutting edge assays with significant biomedical research and clinical utility. Our devices and assays are developed to make a unique and positive impact on medical outcomes.<br>
<br>
We are seeking an experienced engineer to join our growing & dynamic team! The System Integration Engineer will be responsible for installation and technical support to customers throughout CA. The individual must have strong customer service and presentation skills. This hands-on engineer will also assist in instrument design, develop, integration, testing and documentation.  Must be able to effectively and accurately troubleshoot, be self-motivated and able to operate independently in a laboratory environment. <br>
<br>
Other Essential Duties: <br>
•	Assist in instrument design, development and integration.<br>
•	Test, analyze and validate instrument’s performance.<br>
•	Instrument maintenance and documentation  <br>
•	Install instrument and provide technical support to Celula’s customers.<br>
•	Perform other duties as assigned.<br>
<br>
Qualifications:  <br>
•	Master’s degree in Engineering required.<br>
•	Minimum 5 year’s of system design, develop and integration experience.<br>
•	Solid understanding of engineering principals – including optical, mechanical and electrical components/systems.<br>
•	Hands-on experience in instrument integration, installation and testing.<br>
•	Experience of design and develop bio-instrument is a plus.<br>
•	Must have effective written and verbal communications skills.<br>
•	Excellent customer service and presentation skills and the ability to effectively interact with a diverse client base. <br>
•	Up to 50% travel required<br>
•	Must have valid driver’s license, good driving record and comprehensive auto insurance.  <br>
<br>
Celula, Inc. offers a competitive compensation and benefits package, including medical, dental, vision, life, long term care, disability, flex spending accounts, 401k and stock options. Please send resume and cover letter to: hr@celula-inc.com See our website...www.celula-inc.com<br>
<br>
<br>
]]></description>
<dc:date>2009-10-29T17:10:41-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1443582226.html</dc:source>
<dc:title><![CDATA[System Integration Engineer (Contract: 20 hours per week)  (San Diego)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-29T17:10:41-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1443578390.html">
<title><![CDATA[Senior Mechanical Engineer (contract: 20 hour per week)  (San Diego)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1443578390.html</link>
<description><![CDATA[Celula, Inc., a growing San Diego venture backed company, develops innovative instruments for clinical diagnostics and biomedical research using advanced micro-fluidics and other technologies. Celula identifies, develops, and validates unique cutting edge assays with significant biomedical research and clinical utility. Our devices and assays are developed to make a unique and positive impact on medical outcomes.<br>
<br>
We are looking for an experienced Mechanical Engineer to join our growing and dynamic team!  The candidate will perform mechanical design and assembly for Celula’s bio-instrument development and manufacturing. This hands-on engineer must be self-motivated, able to operate independently in a laboratory environment, and must also be able to communicate and interact well in a team environment.<br>
<br>
<br>
Other Essential Duties: <br>
•	Designs, develops, modifies, assemblies and evaluates mechanical components and system.<br>
•	Create detailed fabrication and assembly drawings.<br>
•	Manage the design documentation and control process.<br>
•	Provides support to other engineering team members in mechanical design and components selection.<br>
•	Performs other duties as assigned.<br>
<br>
Qualifications: <br>
•	BSME or higher.<br>
•	Minimum 10 year’s of mechanical design experience.<br>
•	Solid understanding of mechanical engineering principles.<br>
•	Solid understanding of design and testing philosophies and methods.<br>
•	Solid understanding of design document requirements.<br>
•	Design experience of injection molding parts.<br>
•	Excellent written and verbal communication skills. <br>
•	Proficient in mechanical design software, Solid Works preferred.<br>
<br>
Celula, Inc. offers a competitive compensation and benefits package, including medical, dental, vision, life, long term care, disability, flex spending accounts, 401k and stock options. Please send resume and cover letter to: hr@celula-inc.com See our website...www.celula-inc.com<br>
<br>
]]></description>
<dc:date>2009-10-29T17:07:19-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1443578390.html</dc:source>
<dc:title><![CDATA[Senior Mechanical Engineer (contract: 20 hour per week)  (San Diego)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-29T17:07:19-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1443569683.html">
<title><![CDATA[Principal Scientist, Biochemistry Assay Development (San Diego )]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1443569683.html</link>
<description><![CDATA[Celula, Inc., a growing San Diego venture backed company, develops innovative instruments for clinical diagnostics and biomedical research using advanced micro-fluidics and other technologies. Celula identifies, develops, and validates unique cutting edge assays with significant biomedical research and clinical utility. Our devices and assays are developed to make a unique and positive impact on medical outcomes.<br>
<br>
We are seeking an experienced professional to join our growing and dynamic team! The Biochemistry Assay Development Scientist will lead an interdisciplinary team of biologists, engineers and chemists and will contribute to a variety of development projects.   This hands-on scientist will devise and conduct experiments, then analyze and summarize experimental results as supervisor of a group of Research Associates & Scientists. This individual will also interact with a diverse group of Engineering and Biology scientists as part of a multidisciplinary team. <br>
<br>
Other Duties include: <br>
<br>
&#61556;	Devise, direct, and perform PCR or similar enzymatic chemistry experiments on both commercial platforms and Celula¹s proprietary instruments.<br>
&#61556;	Test, calibrate and improve liquid handling instrumentation and processes.<br>
&#61556;	Develop SOPs for novel assays.<br>
&#61556;	Troubleshoot and improve process efficiency.<br>
&#61556;	Support additional chemistry and engineering development projects<br>
&#61556;	Other duties and projects as assigned. <br>
<br>
Qualifications:<br>
&#61556;	Ph.D. in Molecular Biology, Biochemistry, or Chemistry required.<br>
&#61556;	Minimum 8 year’s of experience in biochemistry process/assay development required. <br>
&#61556;	Proven track record in solving complex technical issues.<br>
&#61556;	Experienced and knowledgeable in micro/nano scale liquid dispensing and handling, imaging analysis and thermal control.<br>
&#61556;	Experience and expertise in molecular assays, particularly DNA or RNA based, including fundamental knowledge and experience with reaction chemistry and optimization.<br>
&#61556;	Excellent ability to communicate and collaborate in a team environment.<br>
&#61556;	Excellent computer skills required for experiment planning, data analysis and reporting.<br>
&#61556;	Programming skills /experience required for instrument control; Labview experience is a plus.<br>
<br>
Celula, Inc. offers a competitive compensation and benefits package, including medical, dental, vision, life, long term care, disability, flex spending accounts, 401k and stock options. Please send resume and cover letter to: hr@celula-inc.com See our website...www.celula-inc.com<br>
<br>
<br>
<br>
]]></description>
<dc:date>2009-10-29T17:00:01-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1443569683.html</dc:source>
<dc:title><![CDATA[Principal Scientist, Biochemistry Assay Development (San Diego )]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-29T17:00:01-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1443020398.html">
<title><![CDATA[QC Technician I (Sorrento Valley)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1443020398.html</link>
<description><![CDATA[InVivoScribe Technologies, a rapidly growing and profitable biotechnology company, has an immediate opening for a full-time QC Technician I.  Candidates must have excellent written and verbal communication skills, a strong work ethic, a high attention to detail, computer literacy, and the ability to work independently following verbal instructions and SOPs. <br>
<br>
Primary Duties and Responsibilities include the following:<br>
•	The Technician is responsible for assuring that only quality products are released for distribution. It is their job to ensure that products are tested to meet the applicable government regulations and industry standards<br>
•	Effectively implement and maintain the company's standard operating procedures for Quality Control.<br>
•	Conduct in-process and final product testing and generate testing results reports. <br>
•	Review, and verify quality control and technical service documents (standard operating procedures, QC testing procedures, acceptance criteria, etc.) for IVS products.  <br>
•	Maintain inventory levels of raw materials used in quality control.<br>
•	Be able to use Adobe Acrobat, Illustrator, and Photoshop for art work and graphics in documents.  <br>
<br>
Requirements:<br>
•	Requires knowledge and skills normally acquired through the successful completion of a BS Degree in a scientific discipline. <br>
•	Attention to detail.<br>
•	Ability to follow Standardized Operating Procedures (SOPs).<br>
•	The ability to work independently as well as in a team environment.<br>
•	Excellent communication skills with the ability to train employees. <br>
•	The ability to manage multiple projects and changing priorities.<br>
•	Willingness to learn and take on new challenges.<br>
•	Ability to perform some tasks that are monotonous & physically demanding in lab environment.  <br>
•	Occasional lifting of up to 30 pounds.<br>
•	Some activities will take place at a desk and on a computer.<br>
<br>
Skills, Knowledge & Abilities Preferred, but not Required:<br>
•	1-2 years of experience in a GMP regulated industry or equivalent combination of education and experience is beneficial.<br>
•	Working knowledge of polymerase chain reactions, gel electrophoresis, capillary electrophoresis, DNA/RNA isolation and purification, and cDNA synthesis is beneficial.<br>
•	Experience with Adobe software.<br>
•	Inventory maintenance experience.<br>
<br>
FAX/email resume to 858-623-8109 or HR@invivoscribe.com. <br>
Please, no phone calls or walk-ins about this job!<br>
<br>
Salary: Commensurate with experience<br>
]]></description>
<dc:date>2009-10-29T10:57:40-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1443020398.html</dc:source>
<dc:title><![CDATA[QC Technician I (Sorrento Valley)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-29T10:57:40-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1443018133.html">
<title><![CDATA[PRODUCTION ASSOCIATE I (Sorrento Valley)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1443018133.html</link>
<description><![CDATA[InVivoScribe Technologies (IVS), a privately-held biotechnology company headquartered in San Diego, California, is a world leader providing a comprehensive selection of standardized PCR-based gene rearrangement, chromosome translocation, and gene mutation testing products and controls to the hematopathology community.<br>
<br>
We have an immediate opening for a Full-Time Production Associate I. <br>
<br>
Duties and Responsibilities include the following:<br>
•	Primary job duties focus on tissue culture, DNA/RNA isolation/purification/quantification, and supportive administrative tasks.   <br>
•	Follow cGMP guidelines to manufacture products using batch records and SOPs, which include labeling, formulating, filling products, and etc.  <br>
•	Make detailed observations, analyze data and interpret results. <br>
•	Collect data following established design controlled protocols.<br>
•	Ensure the production/laboratory environment is maintained consistent with SOPs, operating practices and regulatory requirements.<br>
•	Accurately aliquot bulk reagents using aseptic techniques.<br>
•	Maintain production reagents and notify specific personnel in case of shortages.  <br>
•	Assist in writing regulatory documents, including batch records, SOPs, and purchasing specifications.<br>
•	Improve process and optimize laboratory production programs, processes and procedures.<br>
•	Conduct laboratory analysis and maintain standard production documentation records for production programs, projects and activities.<br>
•	Prepare buffers and reagents for production.<br>
•	Maintain lab areas and cleanliness.<br>
•	Maintain lab equipment and monitor temperature/pressure in specified areas.<br>
•	Other duties and responsibilities will be given as experience is acquired.<br>
<br>
Requirements:<br>
•	BS in Biological Science or Chemistry.<br>
•	A minimum 1 to 2 years work experience in a cGMP manufacture environment or laboratory setting.<br>
•	A strong working knowledge of mammalian cell culture and molecular biology. <br>
•	Able to utilize automated or manual laboratory equipment (pipettes, UV spectrophotometer, thermocyclers, etc.).<br>
•	Experience with sterile techniques and accurate pipetting skills a must.<br>
•	Ability to work with PC or Macs.<br>
•	Knowledge of MS Office software and Adobe software (Photoshop and Illustrator). <br>
•	Ability to work independently following verbal and written instructions.<br>
•	Meticulous and detailed oriented. <br>
•	Strong written and communication skills. <br>
•	Ability to perform repetitive work, while maintaining a strong team environment.<br>
•	Good work ethic and ability to train quickly on new tasks and equipment.<br>
•	Ability to recognize deviation from accepted practice is required.<br>
<br>
<br>
PLEASE SPECIFY THE POSITION AND APPLY IN ONE OF THE FOLLOWING WAYS:<br>
•	Submit your resume via email at HR@invivoscribe.com<br>
•	Fax: 858-623-8109<br>
•	Please, no phone calls about this position.<br>
•	Please, walk-ins about this position.<br>
<br>
COMPENSATION: <br>
•	Competitive salary that is commensurate with experience.  <br>
•	IVS provides health, dental, and vision coverage and a 401(k) retirement plan.<br>
]]></description>
<dc:date>2009-10-29T10:56:08-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1443018133.html</dc:source>
<dc:title><![CDATA[PRODUCTION ASSOCIATE I (Sorrento Valley)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-29T10:56:08-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/ssd/sci/1442872719.html">
<title><![CDATA[Researchers (Las Vegas)]]></title>
<link>http://sandiego.craigslist.org/ssd/sci/1442872719.html</link>
<description><![CDATA[Bigelow Aerospace Advanced Space Studies (BAASS), a sister company to Bigelow Aerospace, is a newly formed research organization that focuses on the identification, evaluation, and acquisition of novel and emerging future technologies worldwide as they specifically relate to spacecraft. BAASS is headquartered in Las Vegas, Nevada. We are seeking experienced scientists to join our research teams. If you are an inquisitive outside of the circle thinker, who is detail oriented and who is looking for a challenge, this is a unique and exciting opportunity to advance your career and to be a part of cutting edge research. 
<br>

<br>

<br>

<br>
Numerous positions are available in various fields. 
<br>

<br>

<br>

<br>
Impressive candidates will need to have 10 or more years of research and hands on experience in the disciplines related to aerospace sciences, specifically including: 
<br>

<br>

<br>

<br>
· propulsion 
<br>

<br>

<br>

<br>
· astrophysics 
<br>

<br>

<br>

<br>
· physics 
<br>

<br>

<br>

<br>
· biochemistry 
<br>

<br>

<br>

<br>
· nanotechnologies 
<br>

<br>

<br>

<br>
· microbiology 
<br>

<br>

<br>

<br>
· stealth technologies 
<br>

<br>

<br>

<br>
· and the engineering disciplines 
<br>

<br>

<br>

<br>

<br>

<br>
Several positions are also available for research scientists in the disciplines of: 
<br>

<br>

<br>

<br>
· forensic pathology 
<br>

<br>

<br>

<br>
· electromagnetic fields 
<br>

<br>

<br>

<br>
· biological cognitive interaction 
<br>

<br>

<br>

<br>
A Masters or PhD in a relevant field is a must. Candidates must qualify for secret and top secret clearances and must be willing to submit to a thorough background check. 
<br>

<br>

<br>

<br>

<br>

<br>
For all positions, some travel – both nationally and internationally -- may be required. 
<br>

<br>

<br>

<br>

<br>

<br>
BAASS offers excellent pay and a benefit package that includes: medical, dental, vision, PTO, and a 401k. 
<br>

<br>

<br>

<br>

<br>

<br>
For more information or to submit an application, go to <a href="http://www.bigelowaerospace.com/"  rel="nofollow">http://www.bigelowaerospace.com/</a> or Mail your CV/Resumé to Attn. Donna @ 4640 S. Eastern Ave. Las Vegas, NV 89119 or fax to 702-456-9404. 
<br>

<br>
]]></description>
<dc:date>2009-10-29T09:35:22-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/ssd/sci/1442872719.html</dc:source>
<dc:title><![CDATA[Researchers (Las Vegas)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-29T09:35:22-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1442832390.html">
<title><![CDATA[Process Development Associate II (La Jolla, CA)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1442832390.html</link>
<description><![CDATA[Advanced BioHealing (ABH) is a specialty biotechnology company focused on the development and marketing of cell-based and tissue-engineered products. We are a privately held company with two approved products: Dermagraft® and TransCyte®. Our development pipeline also includes a next-generation bioengineered wound therapy for which two Investigational Device Exemption (IDE) applications have been approved by the Food and Drug Administration (FDA).<br>
<br>
Job Title: 	            Process Development Associate II<br>
Department:            Process Development<br>
<br>
<br>
SUMMARY <br>
<br>
This position is responsible for assisting in several biology/engineering projects to improve current process systems and/or to bring new products to market. The PD Associate II must be able to demonstrate the understanding and use of scientific theory that crosses research techniques.  The PD Associate II demonstrates creativity in troubleshooting and developing new solutions or improving upon existing components, processes and equipment by performing experimental studies, prototyping, and scale-up activities; supporting manufacturing needs; and creating relevant documentation for cGMP compliance. The PD Associate II completes projects with increased independence and self-reliance, and demonstrates teamwork and initiative in the interactions with their co-workers.<br>
<br>
ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.<br>
<br>
% of Time	Job Task<br>
<br>
40%  Designing, writing and executing, documenting, and analyzing experiments/ protocols and associated data; designing, building and refining prototypes; developing parameters for equipment and process validation.<br>
<br>
<br>
20%  Creating supporting documentation for cGMPs including standard operating procedures, batch records, forms, and specifications; creating supporting documentation for validations and qualification tests.<br>
<br>
<br>
15%  Maintaining lab supplies and materials necessary for performing experiments/protocols.  Coordinates preventative maintenance, calibrations, and cleaning as required.<br>
<br>
<br>
15%  Planning and communicating the status, requirements and decision points of current projects with internal department manager(s).<br>
<br>
<br>
10%  Searching for appropriate vendors, materials and components to complete assigned projects.	<br>
<br>
<br>
SUPERVISORY RESPONSIBILITIES <br>
<br>
Position has no FTE supervisory responsibilities; however, may provide guidance and instruction for other Associates or interns, as required.<br>
<br>
QUALIFICATIONS  To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.<br>
<br>
•	Experience/training in cellular/molecular biology, cell culture, and aseptic technique.<br>
•	Ability to summarize and present scientific information, in both written and oral formats.<br>
•	Familiarity with routine laboratory equipment (e.g. centrifuge, analytical balance, pH meter).<br>
•	Design of experiments and statistical analysis and interpretation of results.<br>
•	Organizational skills and ability to complete assignments/tasks with minimal supervision.<br>
•	Computer skills and familiarity with Microsoft Word, Excel, PowerPoint, graphing software and statistical analysis software.<br>
•	Experience/familiarity with FDA-regulated industries and products.<br>
<br>
EDUCATION and/or EXPERIENCE <br>
<br>
B.S. degree in chemical engineering, bioengineering, or related discipline with minimum of 5 years of professional experience.<br>
M.S. degree in chemical engineering, bioengineering, or related discipline with minimum of 2 years of professional experience.<br>
<br>
LANGUAGE SKILLS <br>
<br>
Ability to read, analyze, and interpret professional journals, technical procedures, or governmental regulations.  Ability to write technical reports, business correspondence, and scientific procedures.  Ability to communicate effectively in oral form to present information and respond to questions from vendors, managers, and other functional areas within the company.<br>
<br>
MATHEMATICAL SKILLS <br>
<br>
Ability to perform basic scientific/laboratory calculations, statistical analysis, and an understanding of significant digits and scientific notation.  Ability to use statistical and graphing software to present experimental findings.<br>
<br>
REASONING ABILITY <br>
<br>
Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.  Ability to establish hypothesis-driven experimental designs and follow scientific principles in analyzing and interpreting data.<br>
<br>
CERTIFICATES, LICENSES, REGISTRATIONS <br>
<br>
None required.<br>
<br>
PHYSICAL DEMANDS  The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.<br>
<br>
Routine laboratory benchwork will be required (including standing, repetitive motions, and lifting up to 50 lbs).  Ability to use appropriate personal safety protective equipment and work with various chemicals and hazardous materials.  Must be willing to work in an clean room environment, including following gowning requirements.<br>
<br>
<br>
Please review our website at www.advancedbiohealing.com for more company information.<br>
We offer a competitive benefits & compensation package!<br>
All qualified resumes should be submitted directly to careers@advancedbiohealing.com<br>
<br>
We are an Equal Opportunity Employer.<br>
]]></description>
<dc:date>2009-10-29T09:12:54-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1442832390.html</dc:source>
<dc:title><![CDATA[Process Development Associate II (La Jolla, CA)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-29T09:12:54-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1442807140.html">
<title><![CDATA[Maintenance Mechanic  (La Jolla, CA)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1442807140.html</link>
<description><![CDATA[Advanced BioHealing (ABH) is a specialty biotechnology company focused on the development and marketing of cell-based and tissue-engineered products. We are a privately held company with two approved products: Dermagraft® and TransCyte®. Our development pipeline also includes a next-generation bioengineered wound therapy for which two Investigational Device Exemption (IDE) applications have been approved by the Food and Drug Administration (FDA).<br>
<br>
Job Title: 	Maintenance Mechanic <br>
Department:	Facilities	<br>
<br>
<br>
SUMMARY <br>
<br>
This position maintains and tests mechanical equipment, machinery, and components. Identifies parts or machines that need new parts or need to be replaced and places orders as necessary.  Maintains all logs and required documentation. Provides input along with recommendations for solutions to technical problems. Perform continuous monitoring of equipment status, condition and location.<br>
<br>
ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.<br>
<br>
•	Perform preventive maintenance on laboratory equipment as well as facility support equipment.  Ensure work meets QSR standards.<br>
•	Perform corrective maintenance and trouble shoot production and facility support equipment.  Ensure work meets QSR standards.<br>
•	Perform updates and changes to equipment as needed.  Ensure work meets QSR standards<br>
•	Oversee contractors supporting maintenance activities.<br>
•	Assist in writing and up-dating SOPs and all other related facilities documentation.<br>
•	Respond to process equipment alarms and participate in “on-call” duties.<br>
•	Performs general facility maintenance to include:  painting, wall repair, general plumbing tasks, light replacement and repair.  Follows all company safety compliance procedures.<br>
•	Handles conference room and office set ups as needed.  Performs general housekeeping of buildings and grounds as needed.<br>
•	Performs other assignments as directed by manager.<br>
<br>
QUALIFICATIONS  To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.<br>
<br>
EDUCATION and/or EXPERIENCE <br>
<br>
Requires a high school diploma or equivalent with a minimum of 3 - 5 years related experience.  Formal training in an area of specialty preferred. Must have demonstrated the ability to perform facilities mechanical work.  This includes work with HVACR and central plant equipment.  Proven ability to work safely around 120 and 277 VAC power applications is preferred.  Working knowledge of GMP and GLP requirements.  Familiar with FDA, ISO, and other regulatory agency requirements a plus.  Good computer skills are required.  Establishing and maintaining cooperative working relationships with individuals contacted in the course of work. Strong customer service skills are necessary. Strong organizational skills and neat handwriting is needed.  Strong communication and customer service skills are necessary.   <br>
<br>
LANGUAGE SKILLS <br>
<br>
Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals.  Ability to write routine reports and correspondence.  Ability to speak effectively before groups of customers or employees of organization.<br>
<br>
MATHEMATICAL SKILLS <br>
<br>
Ability to calculate figures and amounts such as discounts, interest, commissions, proportions, percentages, area, circumference, and volume.  Ability to apply concepts of basic algebra and geometry.<br>
<br>
REASONING ABILITY <br>
<br>
Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.  Ability to define problems, collect data, establish facts, and draw valid conclusions<br>
<br>
<br>
PHYSICAL DEMANDS  The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.<br>
<br>
Ability to gown in a full laboratory suit, climb ladders, lift 50 lbs without assistance, bend, and stand for long periods of time. Will work with 70% IPA solution, bleach, various lubricants, paint, and other household type cleaning agents. Must be available for work outside of traditional business hours and overtime.  Must be available to participate in the “on-call” duties.  <br>
<br>
<br>
Please review our website at www.advancedbiohealing.com for more company information.<br>
We offer a competitive benefits & compensation package!<br>
All qualified resumes should be submitted directly to careers@advancedbiohealing.com<br>
<br>
We are an Equal Opportunity Employer.<br>
]]></description>
<dc:date>2009-10-29T08:58:32-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1442807140.html</dc:source>
<dc:title><![CDATA[Maintenance Mechanic  (La Jolla, CA)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-29T08:58:32-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1442777458.html">
<title><![CDATA[Statistical Programmer (CA)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1442777458.html</link>
<description><![CDATA[Acclaimed by its clients as one of the best niche providers in the clinical research industry, Instat Services, Inc. provides superior biostatistics and statistical programming services and we are now recruiting for a full-time Statistical Programmer to join our team. <br>
<br>
The qualified candidate should have training equivalent to a BS, MS preferred, in Life Sciences, Computer Science, Statistics, or related field and is required to have a minimum of 6 years experience in Statistical Programming using the SAS system in clinical data analysis. Job requirements are as follows: <br>
<br>
•	Very strong SAS programming skills with proficiency in SAS/Base, SAS/Macros, SAS Procedures, SAS data step programming and SAS/Graph. <br>
•	Responsible for planning, writing and executing SAS statistical programs designed to analyze clinical trial data and produce tables, figures and listings. <br>
•	SAS programming support for exploratory analyses, non-clinical analyses & publication analyses. <br>
•	Must have clear verbal and written communication and be able to communicate in a timely manner. <br>
•	Position requires excellent collaborative skills and the ability to manage complexity and change. <br>
•	Strong problem solving and analytical skills are desired. <br>
•	Must be self-motivated and able to work well with little supervision. <br>
<br>
This is not a Corp-to-Corp contract position. ]]></description>
<dc:date>2009-10-29T08:41:24-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1442777458.html</dc:source>
<dc:title><![CDATA[Statistical Programmer (CA)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-29T08:41:24-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1441908460.html">
<title><![CDATA[Research Associate I (Sorrento Valley)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1441908460.html</link>
<description><![CDATA[Accumetrics is a privately held company that is committed to advancing medical understanding of blood platelets and enhancing quality of care for patients at a risk of cardiovascular disease by providing industry-leading diagnostic tests for platelet function assessment.  We are growing and recognize that talented and motivated people working together is the key to our success and growth.  We have an exciting opportunity for a Research Associate I.  Job code 20 MKY.<br>
<br>
Job Summary:  In this role you will work mainly in the lab under limited supervision executing experiments and supporting new product development, scale-up, process optimization, technology transfer, and process validation activities.  Core functions focus on handling and manipulating blood samples, performing assays, processes, experiments and tests as requested in accordance with established procedures in the development and optimization of new products and processes.  You will be required to communicate scientific results in writing and verbally in the appropriate forum.  This is an excellent opportunity for a bright and motivated new graduate!<br>
<br>
Requirements:   <br>
•	BS degree in Biology, Molecular Biology, Biochemistry or Chemistry.<br>
•	0-2 years of diagnostic product development experience in an FDA regulated environment. <br>
•	Technical working knowledge in protein chemistry, reagent formulation and process development and optimization.<br>
•	Experience with the handling and manipulating of blood and/or platelets is preferred. <br>
•	Able to communicate and present technical information effectively verbally and in writing and to follow both written and verbal instructions. <br>
•	Proficient computer skills and good working knowledge of MS Office and general database usage. <br>
<br>
Come be a part of the team at Accumetrics and see your career grow.  We are located in the Sorrento Valley area and offer great benefits and a challenging, pleasant work environment.  Please forward you resume and salary history to:  jobs@accumetrics.com and reference Job Code 20 MKY<br>
]]></description>
<dc:date>2009-10-28T14:33:39-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1441908460.html</dc:source>
<dc:title><![CDATA[Research Associate I (Sorrento Valley)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-28T14:33:39-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1441505376.html">
<title><![CDATA[Informatics Scientist  (San Diego, CA)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1441505376.html</link>
<description><![CDATA[Consider the opportunities at <b>SEQUENOM</b>, a life sciences company committed to providing the best genetic analysis products that translate the results of genomic science into solutions for molecular diagnostics, biomedical research, translational research and molecular medicine applications. As an industry innovator, our employees are on the forefront from basic research to revolutionary diagnostics.  Our employees are the building blocks of our success and are rewarded with excellent compensation and benefits and an innovative environment.  Come learn more about SEQUENOM and see what we have to offer.   <br>
 <br>
Reporting to the Senior Director of Bioinformatics, the Informatics Scientist is responsible for developing algorithms and analyzing combinatorics for molecular biology analystis programs and related software.  <br>
 <br>
 <br>
<b>RESPONSIBILITIES:</b><br>
<br>
•	Develops numerical algorithms for simulations, and employs computational mathematics for complex systems. <br>
•	Conducts data mining over internally produced and publicly available data sets. <br>
•	Provides analysis information to management to aid in decision making on the development of new products <br>
•	Works with software development staff to support migration of developed tools, algorithms and analytical approaches for use in Sequenom’s software products. <br>
<br>
<br>
<b>REQUIREMENTS: </b><br>
<br>
•	Master's degree required, PhD preferred in Computer Science or related field. <br>
•	Minimum of 6 years work experience with at least 3 in a biotech setting <br>
•	Experience with at least one of the following high level programming languages is required:  R/S-PLUS (preferred), Matlab, Mathematica, Python <br>
•	Demonstrated experience with combinatorial optimization techniques is required<br>
•	Experience with biological sequence analysis <br>
•	Strong writing, organization and communication skills. <br>
•	Programming experience in C++, Java, or Perl and experience with databases and SQL highly desirable. <br>
•	Candidates must be able to work in a collaborative research environment and must provide evidence of relevant research expertise in the form of technical publications, presentations, software, and/or knowledge of applications. <br>
<br>
To apply, please visit <a href="http://www.sequenom.com/Corporate/Careers/Jobs"  rel="nofollow">http://www.sequenom.com/Corporate/Careers/Jobs</a>  .<br>
 <br>
EEO/AAP<br>
]]></description>
<dc:date>2009-10-28T10:39:21-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1441505376.html</dc:source>
<dc:title><![CDATA[Informatics Scientist  (San Diego, CA)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-28T10:39:21-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1441457661.html">
<title><![CDATA[Part Time Pharmaceutical Service Technician (Chula Vista)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1441457661.html</link>
<description><![CDATA[Part-Time Pharmaceutical Service Technician<br>
<br>
 	WHO WE ARE<br>
Profil Institute for Clinical Research Inc. (PICR) is an independent research institute conducting clinical phase I-II trials, primarily in diabetes and carbohydrate metabolism, under contract to the biopharmaceutical industry [www.profil-research.com]. <br>
<br>
 	THE POSITION<br>
PICR is seeking a part-time Pharmaceutical Service Technician to provide pharmacy support at PICR. Hours are primarily weekends and some weekday evenings.<br>
 Key Responsibilities will include:<br>
 	Receives, labels, stores, organizes and returns/destroys study medications for clinical trials.<br>
 	Prepares and updates all drug inventory logs and is current with all clinical trial drug preparation schedules.<br>
 	Assists with the preparation, labeling, dispensing and recording of study drugs.<br>
 	Assists with the ordering, organizing, and inventorying of concomitant medications.<br>
 	Serves as an unblinded staff member to meet the requirements of specific protocols.<br>
<br>
 	WHO YOU WOULD NEED TO BE<br>
The ideal candidate would someone who is/has: <br>
 	Nationally or state licensed or certified pharmacy technician or equivalent.<br>
 	The ability to perform all the pharmacy related procedures<br>
 	the understanding of sterile technique preferred<br>
 	The ability to respect subject confidentiality and blinding procedures<br>
 	the understanding of medical terminology and calculations      <br>
 	Excellent organizational skills<br>
 	The ability to work as a team member<br>
 	Attention to detail <br>
Join PROFIL: <br>
 	A vibrant, growing organization<br>
 	A dynamic, enthusiastic work environment<br>
 	A team of committed and dedicated colleagues <br>
 	Be involved at the leading edge of medical therapeutic research.<br>
]]></description>
<dc:date>2009-10-28T10:13:58-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1441457661.html</dc:source>
<dc:title><![CDATA[Part Time Pharmaceutical Service Technician (Chula Vista)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-28T10:13:58-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/esd/sci/1441338891.html">
<title><![CDATA[Senior Chemist - Diagnostic Kit Manufacturing- 2nd shift (Santee )]]></title>
<link>http://sandiego.craigslist.org/esd/sci/1441338891.html</link>
<description><![CDATA[Scantibodies Laboratory, the 6th largest Biotech company in San Diego is looking for a Senior Chemist for the 2nd shift in the Diagnostic Kit Manufacturing Department. 
<br>


Summary:  Senior Chemist V position requires that the employee have an excellent understanding of scientific principles as well as strong technical skills for solving problems and working with complex R&D projects.  This position is necessary for assay development, R&D optimization projects, manufacture of complex controls and standards, and troubleshooting for existing protocols and processes.


Essential Duties:						
Familiarity with iodinations for all kit manufacturing which include ACTH, PTH and Calcitonin.  This responsibility includes job order production and management, understanding of radiation and its effects, general knowledge of how radiation is used in IRMA assays.	


Research and Development for assay development, kit optimizations, controls and standards, etc.  This can include studies involving stability of kit components or controls and standards, minimizing variances between production lots, optimizing component performance and assisting the R&D team as needed for project support. Troubleshooting and optimizing of existing protocols and processes for kits manufacture and the manufacture of controls and standards.	

Technical and mechanical responsibilities such as tube coating, plate coating, freeze driers, etc.	
Manufacturing of complex controls and standards, including but not limited to cancer antigen controls, serum protein controls, and multianalyte controls.  Manufacturing of kit components such as ELISA and ICMA plates, standards, controls, conjugates, wash buffers, etc.  	


Equipment Used:  
Laboratory Computer (Word, Excel, M2M)
Tube Coater
Gamma Counter
ELISA plate coater
Luminometer
Plate/Tube Washer
General Laboratory Equipment (i.e. pipettes, pumps, filling systems, etc.)  
			

Job Specifications:  
Minimum Bachelor’s degree in Biology, Chemistry or Biochemistry.  Preferred MS in similar field.

Benefits Include: Medical, Dental, 401K, tuition reimbursement and incentive compensation. 

]]></description>
<dc:date>2009-10-28T09:10:05-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/esd/sci/1441338891.html</dc:source>
<dc:title><![CDATA[Senior Chemist - Diagnostic Kit Manufacturing- 2nd shift (Santee )]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-28T09:10:05-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/esd/sci/1441337442.html">
<title><![CDATA[Regulatory Affairs Manager (Santee)]]></title>
<link>http://sandiego.craigslist.org/esd/sci/1441337442.html</link>
<description><![CDATA[Scantibodies Laboratory, Inc., one of the largest Biotech comapnies in San Diego is currently recruiting for a Manager of Regualtory Affairs. 
<br>

<br>
Description: Ensure that Scantibodies obtains and maintains all regulatory approvals of products and facilities. This person is a key driver of change within Scantibodies and is heavily focused on Improvements to products and processes. Experience must include 510K filings for in-vitro diagnostic devices or medical devises, Submission of pre-IND, IND, NDA/BLA applications for drugs and biologics, developing a regulatory strategy for the regulated products which ensures compliance with regulations and marketability of products. Management of Department personnel. 
<br>
 
<br>
Requirements: Bachelors Degree, minimum of 7 years experience in regulatory affairs in similar industry, knowledge of GMP/QSR and ISO international regulations and standards which apply to SLI. Computer literate in MS Word and Excel and possess excellent communication skills. 
<br>
 
<br>
Benefits Include: Medical, Dental, 401K with company match, tuition reimbursement and incentive compensation. 
<br>

<br>
visit our website at:  www.scantibodies.com
<br>

<br>
]]></description>
<dc:date>2009-10-28T09:09:21-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/esd/sci/1441337442.html</dc:source>
<dc:title><![CDATA[Regulatory Affairs Manager (Santee)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-28T09:09:21-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/esd/sci/1441335461.html">
<title><![CDATA[Validation Specialist (Santee)]]></title>
<link>http://sandiego.craigslist.org/esd/sci/1441335461.html</link>
<description><![CDATA[Scantibodies Laboratory, Inc., one f the largest Biotech companies in San Diego is curretnly looking for a Validation Specialist to join our Regulatory team.
<br>

<br>
Description: Responsible for all aspects of Validation across all of the Scantibodies product lines which includes diagnostics, biologics and therapeutics. This position will proactively identify plans to identify equipment, processes, and computer systems. Develop necessary protocols to challenge the process to meet regulatory requirements and assure that the process is reproducible. 
<br>
 
<br>
Requirements: Bachelors Degree or equivalent work experience, 5 years experience in biologics/pharmaceuticals or diagnostics. 3 years in a validation role. Detailed knowledge of GMP and ISO regulations and standards as they apply to the manufacturing of biologics/pharmaceuticals and/or diagnostics 
<br>

<br>
Benefits Include: Medical, Dental, 401K, tuition reimbursement and incentive compensation. 
<br>

<br>
]]></description>
<dc:date>2009-10-28T09:08:18-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/esd/sci/1441335461.html</dc:source>
<dc:title><![CDATA[Validation Specialist (Santee)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-28T09:08:18-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1441230054.html">
<title><![CDATA[Associate Scientist(Immuno) (Mira Mesa)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1441230054.html</link>
<description><![CDATA[Leading biotech company in Mira Mesa seeks an Associate Scientist. This position is responsible for the manufacturing and testing products in the Immunochemicals product line. Techniques include buffer preparation, SDS-PAGE, Western Blotting, ELISA, antibody purification/conjugation and mammalian cell culture. Other duties includes: vialing, packaging and general laboratory oraganization. Qualified candidate will have a B.S. or B.A. in a life science or related field and 4-6 years actual working experience. Must be proficient in the use of computers and general laboratory equipment. Experience writing and/or revising SOPs and work instructions. Overtime required through the end of the year. Please submit your resume for immedidate consideration. ]]></description>
<dc:date>2009-10-28T08:07:40-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1441230054.html</dc:source>
<dc:title><![CDATA[Associate Scientist(Immuno) (Mira Mesa)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-28T08:07:40-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1441075024.html">
<title><![CDATA[Environmental Professional (subcontractor) (San Diego)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1441075024.html</link>
<description><![CDATA[Environmental Professional (subcontractor)<br>
<br>
Position Description<br>
EBI Consulting is seeking Environmental Professionals on a part-time/contactor basis to complete Phase I Environmental Site Assessment reports and/or wireless National Environmental Policy Act (NEPA) reports throughout the United States.   The work will require completion of field inspections of various property types, primarily sites under consideration for telecommunications installation as well as completion of independent research of local, state, and federal resources in compiling the information required for Phase I ESAs and NEPA Related Reports.  In addition, screening for Lead Containing Pain and Asbestos may be required.   <br>
<br>
Experience Required<br>
Prior experience with Phase I Environmental Site Assessments and NEPA Reports conducted for wireless carriers, tower companies, acquisition firms, or lenders. <br>
<br>
A professional science degree in environmental science, ecology, biology, geology, engineering, or related field, and over two years professional experience in NEPA consulting and/or due diligence. <br>
<br>
An understanding of and experience with NEPA reviews for proposed construction projects, including evaluating impacts to floodplains, wetlands, endangered species habitats, and historic properties<br>
LBP and ACBM Certifications a PLUS.<br>
<br>
Submittal<br>
Please submit a resume and cover letter in Word or PDF format via email to jobs@ebiconsulting.com.  You must include the following information:<br>
<br>
1. Reference job #, job title and resource<br>
2. Brief summary of past related experience (highlight your experience as it relates to our need & industry);<br>
3. List of your education credentials and professional registrations<br>
4. Salary history<br>
<br>
We look forward to hearing from you!<br>
]]></description>
<dc:date>2009-10-28T06:10:40-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1441075024.html</dc:source>
<dc:title><![CDATA[Environmental Professional (subcontractor) (San Diego)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-28T06:10:40-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1440628980.html">
<title><![CDATA[In vitro Assay Development Specialist (La Jolla, CA)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1440628980.html</link>
<description><![CDATA[Burnham Institute for Medical Research, an independent, non-profit, public-benefit basic research organization, located in La Jolla, California, is seeking an In vitro Assay Development Specialist.<br>
<br>
<br>
The Conrad Prebys Center for Chemical Genomics (CPCCG) is seeking a highly-qualified Assay Development Specialist to join our team. The CPCCG is part of the Molecular Library Probe Production Center Network (MLPCN), whose main focus is to generate chemical probes for deciphering the biological functions of novel cellular and biochemical targets and pathways. We are looking for a highly talented, enthusiastic individual who thrives on high-impact projects and takes pride in his/her day-to-day work and accomplishments to join our HTS Assay Development team. This individual will work with other scientists on the development, optimization and implementation of in vitro biochemical assays for high-throughput screening, as well as perform dose response and secondary screens.<br>
<br>
A BS/MS degree and at least 5 years of post-baccalaureate experience in biochemistry or molecular pharmacology are required. Previous experience in the development of diverse biochemical assays with automated well plate preparation and liquid handling instruments is highly beneficial. Knowledge of enzymology and molecular biophysics is essential. Previous work in matrix teams is highly beneficial.<br>
<br>
Burnham Institute for Medical Research offers a competitive salary and benefit package. To apply please visit us online at <a href="http://www.burnham.org."  rel="nofollow">http://www.burnham.org.</a> EOE.<br>
]]></description>
<dc:date>2009-10-27T17:13:15-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1440628980.html</dc:source>
<dc:title><![CDATA[In vitro Assay Development Specialist (La Jolla, CA)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-27T17:13:15-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1440610508.html">
<title><![CDATA[Supervisor, Document Control/Product Release (Sorrento-Mesa)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1440610508.html</link>
<description><![CDATA[ DexCom, Inc. has an immediate job opportunity for an experienced Supervisor, Document Control!  This business has grown with pride, integrity and a focused vision and is seeking service-focused individuals to continue the growth of our reputation.  We are committed to developing technologies and products that improve the lives of people with diabetes.  DexCom has ambitious plans to keep learning and growing – and is seeking people who have the same goals for themselves.  <br>
<br>
This is a unique opportunity to help thousands of people lead a more normal and healthy life, previously not possible before technology existed, while joining an exciting company that is a leader in continuous glucose monitoring.  We are committed to delivering the best in class products and excellent support services to our customers.  <br>
<br>
ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Additional responsibilities may be assigned as needed.<br>
<br>
•	Plan, process and coordinate preparation of documentation projects such as Engineering Control.<br>
•	Support, as needed, documentation processing requirements for each phase of the design and manufacturing process<br>
•	Prepare and coordinate complex change order through implementation with high accuracy.<br>
•	Support manufacturing operations by creating, processing, distributing and controlling revisions of all manufacturing documentation.<br>
•	Support the development of documentation and configuration control procedures.<br>
•	Maintain training records for all employees (including external training and certifications).<br>
•	Preparing and maintaining Batch Records (Lot History Records).<br>
•	Monitoring status of in-process document changes to ensure timely revisions.<br>
•	Maintains establishment and improvement of quality systems and facilitate continuous quality improvements in DexCom Inc’s continuous efforts to improve the Quality System.<br>
•	Maintains and continuously improves document control/Training Records system and SOP’s per FDA regulation standards requirements.<br>
•	Maintains and continuously improves Product Release system and Good Documentation Practices <br>
•	Processing Non-conformances, and Change Order<br>
•	Create / Chaired cross-functional teams to develop and deploy policy, and training Standard Operating Procedure.<br>
•	Create and support Training documentation compliance and record keeping.<br>
•	Oversee the maintenance of the filing system for Quality Record master drawings, CO’s, Specifications, SOP’s, etc., as required. Issue controlled and uncontrolled documents.<br>
•	Responsible for Change Order Board Administration. Reviews CO’s for accuracy, Monitor and follow-up on the status of required action.<br>
•	Review incoming and outgoing documents such as bill of material, drawings, MPI’s, SOP’s, Specifications, schematic, etc., to ensure completeness and appropriateness prior to data entry.<br>
•	Initiates, Implements and releases Change Order.<br>
•	Conduct record review and product release in support of on-going internal/external clinical trials.<br>
•	Perform Agile training on a need basis.<br>
•	Ensure all documentation is legible, complete and correct per current Good Manufacturing Practices (GMP).<br>
•	Reviewing Batch Records.<br>
<br>
REQUIREMENTS<br>
<br>
•	Associate’s degree (A.A) or equivalent from two-year college or technical school; or a minimum of five years - ten years related experience and/or training in Quality System; or equivalent combination of  education and experience. <br>
•	Supervisory experience and demonstrated leadership skills<br>
•	Basic computer skills in Microsoft Word, Excel; Solid Work, AutoCAD; Agile; MRP systems. <br>
•	Previous work experience in an ISO9000 or FDA Regulations environment is preferable<br>
•	Thorough knowledge of all aspects of documentation control and change order process. X<br>
•	Aptitude for detail and accuracy, excellent organization skills, data entry experience<br>
•	Ability to identify and resolve problems, ability to handle multiple assignments. <br>
<br>
ABOUT DEXCOM:<br>
<br>
DexCom Inc. is a publicly traded company listed in the NASDAQ stock exchange.  We have been FDA approved and commercially released two generations of continuous glucose monitors.  More company information is available at www.dexcom.com.<br>
<br>
We offer an excellent benefits package including medical, dental, vision, life insurance and long term disability, 401(k), flexible spending account, a discounted employee stock purchase plan, paid time off, on-site fitness center, and a great work environment.<br>
<br>
If you meet the position requirements and have exceptional communications and customer service skills, please submit your resume to: HR@DexCom.com.  Please reference "Supervisor, Document Control" in the subject line and include your salary requirements.  <br>
<br>
]]></description>
<dc:date>2009-10-27T16:59:13-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1440610508.html</dc:source>
<dc:title><![CDATA[Supervisor, Document Control/Product Release (Sorrento-Mesa)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-27T16:59:13-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1439992625.html">
<title><![CDATA[Full Time Sales Person  (Sorrento Valley)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1439992625.html</link>
<description><![CDATA[Full Time Sales Person<br>
<br>
<br>
<br>
AVIVA is a growing privately held company, located in the heart of San Diego's Life Sciences Corridor. AVIVA Biosciences Corporation is a San Diego-based biotechnology company, which provides novel solutions to the drug discovery industry by integrating biochips with cell and tissue biology. Presently we are seeking an outstanding sales person with a proven track record of successful sales to maximize the growth of our service business.<br>
<br>
Incumbent will support AVIVA’s Services department. <br>
Tasks involved will include:<br>
<br>
1- Meet annual sales target<br>
2- Promoting drug discovery services to all levels of Pharmaceutical organizations<br>
3- Supporting Customer Relations<br>
4- Identifying Contacts<br>
5- Presenting at tradeshows <br>
6- Meeting with potential customers<br>
<br>
Experience in selling to Pharmaceutical companies is required. Incumbent will travel ~50% of the time.<br>
 <br>
Starting salary: Base plus commission<br>
<br>
AVIVA is an equal opportunity employer. We offer competitive compensation, excellent benefits, paid time off, plus a stimulating and collaborative work environment. Our culture is team oriented, fostering creativity and open communication. With minimal employee turnover, AVIVA could be the ideal growth opportunity; where you can achieve your career goals. <br>
<br>
Please email or fax your resume or curriculum vitae, along with a cover letter, to us at the address below. Be sure to reference job code # ABC1027SM in the subject line.<br>
<br>
email: hr@avivabio.com<br>
fax: (858) 552-9040 ( Attn. Human Resources)<br>
address: Human Resources - AVIVA Biosciences Corporation 11045 Roselle Street, Suite 100, San Diego, CA 92121 <br>
]]></description>
<dc:date>2009-10-27T10:37:30-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1439992625.html</dc:source>
<dc:title><![CDATA[Full Time Sales Person  (Sorrento Valley)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-27T10:37:30-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1439061727.html">
<title><![CDATA[Scientist / Chemist / Biochemist / Biologist (Irvine, CA)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1439061727.html</link>
<description><![CDATA[Branan Medical Corporation, a fast growing, innovative manufacturer of diagnostic test kits located in Irvine, California is actively seeking a qualified applicant for the position of Chemist.<br>
<br>
Responsibilities:<br>
Follow written and oral procedures, record results carefully, and write procedures. Must be able to conduct experiments, perform lab duties, and collect and record data. Must be able to analyze and summarize data. Must be detail -oriented with good communication skills. Team player. <br>
<br>
Qualifications:<br>
BS/BA degree from accredited four year college or university required. Must have experience working in a lab environment. Actual experience in an industrial lab setting, a plus. Motivated to learn, work diligently and independently.  New Graduates okay! Good communication skills in fluent English. <br>
<br>
Will train. Great growth opportunities and working environment.<br>
<br>
If this is you, start your career with us today! Send resume with cover letter. Applications without cover letter will be disregarded. <br>
]]></description>
<dc:date>2009-10-26T16:52:11-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1439061727.html</dc:source>
<dc:title><![CDATA[Scientist / Chemist / Biochemist / Biologist (Irvine, CA)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-26T16:52:11-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1438628914.html">
<title><![CDATA[(20) Healthcare Eligibility Counsultants Needed! (UTC/La Jolla)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1438628914.html</link>
<description><![CDATA[Nation’s leader in reimbursement and health economic consulting seeks (20) representatives with advanced computer skills [familiarity with Word, Excel—knowledge of Oracle databases a plus] to assist patient assistance programs and reimbursement eligibility. This position requires excellent communication skills and ability to multitask in a fast paced environment assisting patients and physicians. <br>
<br>
Paid training with excellent opportunities for growth within a professional, corporate headquarters for individuals with stellar customer service experience. <br>
<br>
All candidates are requires to be flexible Monday thru Friday, 6am to 5pm. Candidates will have a proven track record of outstanding work history with great longevity. Previous experience within a financial, medical, or administrative capacity is a plus. All candidates must be able to pass a full background check and drug screen! <br>
<br>
This is a long term temporary position that could lead to opportunities for further employment within a diverse and stable corporation!<br>
<br>
Send resume today for immediate consideration!<br>
<br>
]]></description>
<dc:date>2009-10-26T12:24:23-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1438628914.html</dc:source>
<dc:title><![CDATA[(20) Healthcare Eligibility Counsultants Needed! (UTC/La Jolla)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-26T12:24:23-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1438429330.html">
<title><![CDATA[Salk Institute for Biological Studies - C178 (La Jolla, CA)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1438429330.html</link>
<description><![CDATA[The Salk Institute is currently seeking a Research Assistant II for the Plant Biology Laboratory - Ecker. Lab research primarily centered on functional genomics studies using the reference plant Arabidopsis thaliana with a focus on understanding of hormone signal transduction pathways.
<p>
<b>Research and lab responsibilities include:</b>
<ul>
<li>Operate high-throughput sequencers (Applied Biosystems - SOLiD and Illumina's Genome Analyzer II)
<li>DNA isolation
<li>Sequencing library construction
<li>Maintenance/ordering of sequencing reagents
<li>Communication with field application specialists from Applied Biosystems and Illumina.
</ul>
<b>Education:</b>BS or BA in Biochemistry, Chemistry, Biological Sciences or related discipline required.
<p>
<b>Experience:</b> At least 2 years of molecular biology laboratory experience required. Familiarity with bioinformatics and/or command line usage is preferred but not required.
Special Requirements: Candidate must be highly organized able to balance multiple demands and changing priorities. Excellent communication skills, both oral and written are also required. Must be willing to work a flexible schedule as needed to accommodate research needs.
<p>
<center><b>Interested applicants should apply online at  <a href="http://salk.edu/careers/staff_positions.html"  rel="nofollow">http://salk.edu/careers/staff_positions.html</a></center></b>



]]></description>
<dc:date>2009-10-26T10:42:40-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1438429330.html</dc:source>
<dc:title><![CDATA[Salk Institute for Biological Studies - C178 (La Jolla, CA)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-26T10:42:40-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1435004577.html">
<title><![CDATA[Laboratory Technician (Sorrento Valley, Mira Mesa, San Diego)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1435004577.html</link>
<description><![CDATA[Phamatech, Inc. is currently seeking Toxicology Lab. Technician I working Monday to Friday, 7:30am-4:00pm in our substance abuse testing laboratory.
<br>

<br>
RESPONSIBILITIES:
<br>
Operate Olympus chemistry analyzers
<br>
Operate digital refractometer
<br>
Operate pH meters
<br>

<br>
QUALIFICATIONS:
<br>
Must have Bachelor's degree in science field
<br>
Laboratory (drug testing) experience preferred
<br>
Must pay high attention to detail
<br>
Strong ability to simultaneously perform multiple duties
<br>
Must have excellent communication skills 
<br>

<br>
Phamatech Inc. is an Equal Opportunity Employer
<br>

<br>
Applicants are encourage to confidentially self-identify when applying.
<br>
Resumes from Staffing Agencies will not be accepted.
<br>
Please submit completed application packet and resume to danielle@phamatech.com
<br>
To obtain application packet, please go to <a href="http://www.phamatech.com/application.html"  rel="nofollow">http://www.phamatech.com/application.html</a>
<br>
]]></description>
<dc:date>2009-10-23T16:27:27-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1435004577.html</dc:source>
<dc:title><![CDATA[Laboratory Technician (Sorrento Valley, Mira Mesa, San Diego)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-23T16:27:27-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1434504027.html">
<title><![CDATA[Purification Chemist (Sorrento Valley)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1434504027.html</link>
<description><![CDATA[Job Summary:  The  Purification Chemist will be responsible for high throughtput purification of  oligonucleotides, peptides or small molecules by IEX-HPLC, RP-HPLC, and PAGE techniques.  The chemist will also be responsible for desalting by G-25 or ethanol precipitation as required.  All procedures will be performed in compliance with IS0 9001 regulations.  Additionally, the purification chemist will be expected to cross train in other areas such as synthesis or QC on an as-needed basis.<br>
<br>
2. Essential Skills and Qualifications<br>
•	Experience with RP-HPLC and IEX-HPLC<br>
•	PAGE purification<br>
•	UV quantitation.<br>
•	Solid phase extraction<br>
•	Desalting by G25 and Ethanol precipitation preferred<br>
•	Manual Conjugations with dyes, enzymes, and other modifiers preferred<br>
•	Above average computer skills using programs such as EXCEL, WORD, Outlook, laboratory LIMS systems<br>
•	Excellent communication skills<br>
•	Excellent attention to detail<br>
•	Ability to work as a team member and collaborate across functional areas<br>
•	Prompt and Accurate recording of production data in LIMS system, batch records and laboratory equipment logs.<br>
EDUCATION<br>
Bachelor’s degree in scientific discipline, preferably chemistry or biochemistry<br>
EXPERIENCE<br>
The successful candidate will have 2-5 years of experience <br>
]]></description>
<dc:date>2009-10-23T11:17:38-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1434504027.html</dc:source>
<dc:title><![CDATA[Purification Chemist (Sorrento Valley)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-23T11:17:38-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/nsd/sci/1434395253.html">
<title><![CDATA[Production Manager (Carlsbad)]]></title>
<link>http://sandiego.craigslist.org/nsd/sci/1434395253.html</link>
<description><![CDATA[North County biotech company has an opening for a conscientious, detailed-oriented person to supervise multiple production teams responsible for serum processing and the manufacture of lyophilized  and liquid controls and calibrators.<br>
<br>
RESPONSIBILITIES will include: <br>
* Manage production staff<br>
* Plasma / Serum processing<br>
* Control / calibrator manufacture:<br>
      + Compounding<br>
      + Filtration<br>
      + Centrifugation<br>
      + Lyophilization<br>
      + Product filling<br>
* Writing of production documentation<br>
* Requesting and ordering supplies and raw materials<br>
* Manufacturing and shift scheduling<br>
* Review customer specifications<br>
<br>
MINIMUM QUALIFICATIONS<br>
 * B.S. Biology, Chemistry, Microbiology, Biochemistry or similar degree<br>
 * Minimum two years experience in the In Vitro Diagnostic industry manufacturing reagents, control sera, lyophilized and liquid controls and calibrators<br>
 * Supervisory experience a MUST<br>
 * Outgoing<br>
 * Focused<br>
 * Able to multi-task<br>
 * Good organizational skills<br>
 * Good computer skills - MS Office and/or Open Office<br>
 * Exceptional math skills<br>
 * Career oriented<br>
<br>
Apply for this position by emailing your resume AND your salary history.  Please NO phone calls.<br>
<br>
<br>
<br>
<br>
]]></description>
<dc:date>2009-10-23T10:22:22-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/nsd/sci/1434395253.html</dc:source>
<dc:title><![CDATA[Production Manager (Carlsbad)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-23T10:22:22-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1434305898.html">
<title><![CDATA[Shipping Clerk Needed Today! (Otay Mesa)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1434305898.html</link>
<description><![CDATA[Dear Shipping Clerks, <br>
<br>
Premier biotech company in Otay Mesa is searching for Shipping Clerks to join their team for 3+ months. Please submit your resume and references as a word document if you are interested in applying. <br>
<br>
Shipping Clerk <br>
Duration: 3+ months (May be extended) <br>
Pay: $11/hr, FIRM <br>
Locations: Otay Mesa <br>
<br>
Description: Unloading boxes, performing shipping tasks, and assisting with other warehouse duties as needed. <br>
<br>
Requirements: High School diploma or equivalent and 1-2 years of relevant experience. Ability to lift 50 pounds. Experience using FedEx and UPS Shipping applications. <br>
]]></description>
<dc:date>2009-10-23T09:37:16-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1434305898.html</dc:source>
<dc:title><![CDATA[Shipping Clerk Needed Today! (Otay Mesa)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-23T09:37:16-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1434253440.html">
<title><![CDATA[QC Inspector  I (la Jolla, CA)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1434253440.html</link>
<description><![CDATA[Advanced BioHealing (ABH) is a specialty biotechnology company focused on the development and marketing of cell-based and tissue-engineered products. We are a privately held company with two approved products: Dermagraft® and TransCyte®. Our development pipeline also includes a next-generation bioengineered wound therapy for which two Investigational Device Exemption (IDE) applications have been approved by the Food and Drug Administration (FDA).<br>
<br>
Job Title: 	                     QC Inspector  I<br>
Department: 	Quality Control <br>
<br>
<br>
SUMMARY<br>
<br>
The primary responsibility of this position is to perform incoming inspection of raw materials; which may include performing some basic laboratory testing such as pH, osmolarity, etc.; initiate nonconforming material and deviation reports; generate QC inspection trend reports for incoming raw materials; revise inspection specifications and procedures, as needed; maintain the raw material database.  All activities must be performed per ABH written procedures and to foster continuous quality improvement in the area of QC inspection.<br>
<br>
ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.<br>
•	Inspects/tests incoming raw materials and in-process products including completing inspection reports and all documents associated in the release of materials. <br>
•	Performs laboratory release testing for raw materials, product, etc., as needed.<br>
•	Assists in the transfer of incoming raw material requirements onto item specification documents, including the initiation of document change requests.  <br>
•	Generates monthly trend reports for incoming raw materials<br>
<br>
<br>
SUPERVISORY RESPONSIBILITIES<br>
<br>
This position has no supervisory responsibilities.<br>
<br>
QUALIFICATIONS   To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.<br>
<br>
Education/Experience:  (Indicate minimum levels required.)<br>
The minimum requirements are:<br>
•	High School Diploma or equivalent.<br>
•	1 year experience in QC Inspection or related regulated environment.<br>
	<br>
	Knowledge:  (Indicated special knowledge/areas of expertise required.)<br>
•	Familiarity with ANSI Z1.4 Sampling Plan and MS Access <br>
•	Basic knowledge of GMP regulations	<br>
		<br>
	Skills/Abilities:  (Includes technical, administrative and behavioral skills.)<br>
•	Ability to recognize defects in materials inspected<br>
•	Ability to work in a fast-paced environment<br>
•	Ability to handle high volume of work and adapt to a rapidly changing environment	<br>
•	Ability to train new staff and operates with minimum supervision<br>
•	Good verbal and written communication skills<br>
•	Competency with computer software programs needed to perform job<br>
<br>
LANGUAGE SKILLS <br>
<br>
Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals.  Ability to write routine reports and correspondence.  Ability to speak effectively before groups of customers or employees of organization.<br>
<br>
MATHEMATICAL SKILLS <br>
<br>
Ability to calculate figures and amounts such as discounts, interest, commissions, proportions, percentages, area, circumference, and volume.  Ability to apply concepts of basic algebra and geometry.<br>
<br>
REASONING ABILITY <br>
<br>
Ability to apply common sense understanding to carry out instructions furnished in written, oral, or diagram form.  Ability to deal with problems involving several concrete variables in standardized situations.<br>
<br>
CERTIFICATES, LICENSES, REGISTRATIONS <br>
<br>
None <br>
<br>
PHYSICAL DEMANDS  The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.<br>
•	Work may involve some lifting up to 50 lbs. <br>
•	Exposure to biohazardous products such as human tissues<br>
•	Works in lab area approximately 10% of the time (gowning may be required)<br>
	<br>
Please review our website at www.advancedbiohealing.com for more company information.<br>
We offer a competitive benefits & compensation package!<br>
All qualified resumes should be submitted directly to careers@advancedbiohealing.com<br>
<br>
We are an Equal Opportunity Employer.<br>
]]></description>
<dc:date>2009-10-23T09:10:27-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1434253440.html</dc:source>
<dc:title><![CDATA[QC Inspector  I (la Jolla, CA)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-23T09:10:27-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1433573803.html">
<title><![CDATA[Assembly Line Operator (Sorrento Valley)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1433573803.html</link>
<description><![CDATA[Assembly line operator position open for candidate with a minimum of two years experience in the healthcare industry.  ]]></description>
<dc:date>2009-10-22T17:52:18-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1433573803.html</dc:source>
<dc:title><![CDATA[Assembly Line Operator (Sorrento Valley)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-22T17:52:18-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1433501210.html">
<title><![CDATA[Medical Doctor (San Diego County)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1433501210.html</link>
<description><![CDATA[Seeking Collaboration with Medical Doctor:<br>
<br>
GenWay Biotech, Inc. is a research and diagnostic company which has been established since 1998.  Our California certified CLIA laboratory is testing blood samples for known tumor markers.  Our mission is to provide regular cancer detection solutions, enabling patients to detect malignancies as early as possible.  <br>
<br>
We are seeking a partnership with a Medical Doctor to:<br>
<br>
·         Review and authorize, when appropriate, patient requisition forms.<br>
·         Review results of tumor marker analysis.<br>
·         Communicate with patients and release test information.<br>
<br>
We believe this is an exciting opportunity for a medical professional to participate in a novel and practical solution which is in the best interest of patients.  For more information about GenWay’s clinical services please visit www.genwaycliaservices.com.<br>
<br>
GenWay complies with all applicable regulations and ethics of the medical profession. <br>
 <br>
<br>
<br>
<br>
]]></description>
<dc:date>2009-10-22T16:52:47-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1433501210.html</dc:source>
<dc:title><![CDATA[Medical Doctor (San Diego County)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-22T16:52:47-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/nsd/sci/1433441883.html">
<title><![CDATA[Buyer/Planner (Rancho Bernardo)]]></title>
<link>http://sandiego.craigslist.org/nsd/sci/1433441883.html</link>
<description><![CDATA[California MedTech, a rapidly growing medical device developer and manufacturer, is seeking an experienced Planner/Buyer to assist our Director of Materials.<br>
<br>
COMPANY BACKGROUND: <br>
<br>
Our Company is a leading ODM (original design manufacturer) of medical and laboratory capital equipment and handheld devices. We help customers rapidly innovate and commercialize high-quality leading edge technologies. Our reputation and track record are unmatched in the industry. We are based in San Diego (Rancho Bernardo) and work with clients throughout California and the US.<br>
<br>
POSITION OVERVIEW:<br>
<br>
Responsibilities include material sourcing, procurement, and managing supplier relationships helping to improve the company’s responsiveness and improve product quality while lowering overall costs.  Work with product development teams and manufacturing to plan, expedite coordinate various manufacturing and supplier activities to assure that the company meets key customer commitments and expectations.  Setup and maintain manufacturing and material planning data, support master production scheduling activities to maximize the effectiveness of the companies MRP planning and inventory management systems.<br>
<br>
RESPONSIBILITIES:<br>
<br>
Schedule production activities and materials to achieve production schedules.<br>
Work with suppliers to assure commitments to schedule, cost, and quality requirements.<br>
Work with development teams to plan, schedule, and coordinate the movement of materials for the timely completion of critical tasks and release of new products.<br>
Identify and develop new supply sources. <br>
Release, schedule, and status purchase orders and work orders.<br>
Establish and maintain key management reports.<br>
Work directly with key clients.<br>
<br>
QUALIFICATIONS:<br>
<br>
Atleast five years procurement and material planning experience working with medical devices and instrumentation.  APICS CPIM a real plus.<br>
Hands-on experience working with MRP systems, scheduling, and exception reporting.<br>
Ability to interact with internal and external customers <br>
Excellent written and spoken communication skills <br>
Proficiency with MS Office Suite ]]></description>
<dc:date>2009-10-22T16:06:25-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/nsd/sci/1433441883.html</dc:source>
<dc:title><![CDATA[Buyer/Planner (Rancho Bernardo)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-22T16:06:25-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1433425822.html">
<title><![CDATA[Quality Assurance Associate  (La Jolla, CA)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1433425822.html</link>
<description><![CDATA[Advanced BioHealing (ABH) is a specialty biotechnology company focused on the development and marketing of cell-based and tissue-engineered products. We are a privately held company with two approved products: Dermagraft® and TransCyte®. Our development pipeline also includes a next-generation bioengineered wound therapy for which two Investigational Device Exemption (IDE) applications have been approved by the Food and Drug Administration (FDA).<br>
<br>
 <br>
Job Title: 	                     Quality Assurance Associate (Document Control)<br>
Department: 	Quality Assurance<br>
	<br>
<br>
SUMMARY <br>
This position supports the different activities within the Quality Assurance Department.  Incumbent is responsible for extensive filing and archiving activities, record entry and maintenance of the training database.  In addition, performs review of intermediate batch records and autoclave runs, and participates in projects within the QA/RA departments.  <br>
<br>
ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.<br>
•	Master Filing – Maintains Hardcopy Master Files up to date.  Distributes new documentation and retrieval of outdated reference copies, and files the “original” documentation.<br>
•	Administration and Maintenance of the Quality System documents.<br>
•	Issuance of lot numbered documents and forms for manufacturing, quality control and other departments on a weekly basis.<br>
•	Performs archiving and Device History Record filing, Off-Site storage program.<br>
•	Filing and Handling of QA/RA document maintenance activities.<br>
•	Schedules periodic review and coordinates with the different responsible departments to ensure compliance.<br>
•	Maintains the training system.  Enter training records, update training matrices and create new files for new employees in the database.<br>
•	Collaborates in different projects within the QA/RA Department.<br>
•	Additional assignments as directed by Supervisor.<br>
<br>
SUPERVISORY RESPONSIBILITIES <br>
Position has no supervisory responsibilities.<br>
<br>
QUALIFICATIONS:  To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.<br>
<br>
EDUCATION and/or EXPERIENCE <br>
Associate's degree from a two-year College; or one to two years related experience and/or training; or equivalent combination of education and experience.  Associate’s Degree preferred.<br>
<br>
KNOWLEDGE AND SKILLS / ABILITIES<br>
&#61607;	Requires strong personal computer skills Keyboarding, Microsoft Office Applications (Access, Excell and Word).<br>
&#61607;	Must be detailed oriented , be able to follow detailed instructions, possess excellent time management skills, be well organized, a self starter and display a professional demeanor wit a high focus on customer service activities / responsibilities.<br>
&#61607;	Ability to follow through and consistently demonstrate that all primary job duties and responsibilities are current and up to date; ability to closely monitor and communicate progress on daily tasks and responsibilities to Management.<br>
&#61607;	Must be able to work as a team member, maintaining day to day activities while being responsive to changing priorities.<br>
&#61607;	Must have strong customer service skills.<br>
&#61607;	Verbal communication skills (English)<br>
&#61607;	Knowledge of Good Manufacturing Practices / Quality System Regulations and ISO Standards preferred.<br>
&#61607;	Must be able to work a consistent schedule to satisfy the Customer Service responsibilities of the job.<br>
&#61607;	Knowledge of electronic document control systems preferred.<br>
<br>
LANGUAGE SKILLS <br>
Ability to read, analyze, and interpret general business procedures, technical procedures, or governmental regulations.  Ability to effectively present information and respond to questions from groups of managers, and employees of the organization.<br>
<br>
MATHEMATICAL SKILLS <br>
Ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations.  Ability to compute rate, ratio, and percent and to draw and interpret bar graphs.<br>
<br>
REASONING ABILITY <br>
Ability to apply common sense understanding to carry out instructions furnished in written, oral, or diagram form.  <br>
<br>
PHYSICAL DEMANDS  <br>
Position requires incumbent to work with personal computers performing keyboarding / typing and data entry.  Extensive filing required.  Some lifting of boxes is necessary. <br>
<br>
<br>
Please review our website at www.advancedbiohealing.com for more company information.<br>
We offer a competitive benefits & compensation package!<br>
All qualified resumes should be submitted directly to careers@advancedbiohealing.com<br>
<br>
We are an Equal Opportunity Employer.<br>
]]></description>
<dc:date>2009-10-22T15:54:16-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1433425822.html</dc:source>
<dc:title><![CDATA[Quality Assurance Associate  (La Jolla, CA)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-22T15:54:16-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1433376327.html">
<title><![CDATA[Quality Assurance Specialist I  (La Jolla, CA)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1433376327.html</link>
<description><![CDATA[Advanced BioHealing (ABH) is a specialty biotechnology company focused on the development and marketing of cell-based and tissue-engineered products. We are a privately held company with two approved products: Dermagraft® and TransCyte®. Our development pipeline also includes a next-generation bioengineered wound therapy for which two Investigational Device Exemption (IDE) applications have been approved by the Food and Drug Administration (FDA).<br>
<br>
Job Title: 	                     Quality Assurance Specialist I (Document Control)<br>
Department: 	Quality System & Quality Assurance<br>
	<br>
<br>
SUMMARY <br>
This position is responsible of the day to day operation of the Document Control function.  Incumbent is responsible for change incorporation, master filing activities and change administration requirements for product documentation and labeling.  Device Master Record and Device History Record file maintenance.  In addition, performs process improvements within the Document Control Area.<br>
<br>
ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.<br>
•	Change Administration – Screens Change Orders (COs) for completeness and accuracy.  Prepares CO packets for review, tracks COs through the review and approval process and coordinates incorporation of approved changes.  Incorporates approved changes / “redlines” to documentation.  Supports Change Control System metrics to allow for monitoring of trends, etc.<br>
•	Administration and Maintenance of the Quality System documents – Ensures authorizations are maintained for Change Control Board (CCB).  Maintains change/revision history, Device History and Device Master Records, Area Reference copies, Oversees Periodic Review documentation, filing and archiving activities.  Manages Off-Site Storage Program.<br>
•	Master Filing – Produces “original” documentation, verifies the correct incorporation of changes, updates Device Master Record as applicable and verifies master filing activities.  Maintains Hardcopy Master Files up to date.  Distributes new documentation and retrieval of outdated reference copies, and files the “original” documentation.<br>
•	Customer Service Activities – Interdepartmental copy requests, internal customer inquiries, expedition of interdepartmental copy requests, support interdepartmental research / investigation activities.<br>
•	Additional assignments as directed by Supervisor.<br>
•	Collaborate with different members of the QA department working in special projects.<br>
•	Issuance of lot numbered documents and forms for manufacturing, quality control and other departments on a weekly basis.<br>
•	Performs archiving and Device History Record filing, Off-Site storage program.<br>
•	Schedules periodic review and coordinates with the different responsible departments to ensure compliance.<br>
•	Maintains the training system.  Enter training records, update training matrices and create new files for new employees in the database.<br>
•	Additional assignments as directed by Supervisor.<br>
<br>
SUPERVISORY RESPONSIBILITIES <br>
Position has no supervisory responsibilities.<br>
<br>
QUALIFICATIONS<br>
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.<br>
<br>
EDUCATION and/or EXPERIENCE <br>
Bachelor's degree from a four-year College and 1 years of experience in a Document Control GMP work environment; or four to two years related experience and/or training; or equivalent combination of education and experience.  Bachelor’s Degree in a scientific discipline preferred.<br>
<br>
KNOWLEDGE AND SKILLS / ABILITIES<br>
&#61607;	Requires strong computer skills, Microsoft Office Applications (Access, Excell and Word).<br>
&#61607;	Must be detailed oriented, be able to follow detailed instructions, possess excellent time management skills, be well organized, a self starter and display a professional demeanor wit a high focus on quality, compliance, and responsibilities.<br>
&#61607;	Ability to follow through and consistently demonstrate that all primary job duties and responsibilities are current and up to date; ability to closely monitor and communicate progress on daily tasks and responsibilities to Management.<br>
&#61607;	Must be able to work as a team member, maintaining day to day activities while being responsive to changing priorities.<br>
&#61607;	Verbal communication skills (English)<br>
&#61607;	Knowledge of Good Manufacturing Practices / Quality System Regulations and ISO Standards required.<br>
&#61607;	Must be able to work a consistent schedule to satisfy the responsibilities of the job.<br>
&#61607;	Knowledge of electronic document systems.<br>
<br>
LANGUAGE SKILLS <br>
Ability to read, analyze, and interpret general business procedures, technical procedures, or governmental regulations.  Ability to write reports and procedures.  Ability to effectively present information and respond to questions from groups of managers, and employees of the organization.<br>
<br>
MATHEMATICAL SKILLS <br>
Ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations.  Ability to compute rate, ratio, and percent and to draw and interpret bar graphs.<br>
<br>
REASONING ABILITY <br>
Ability to apply common sense understanding to carry out instructions furnished in written, oral, or diagram form.  Ability to deal with problems involving several concrete variables in standardized situations.<br>
<br>
PHYSICAL DEMANDS  <br>
Position requires incumbent to work with personal computers performing keyboarding / typing and data entry.  Extensive filing required.  Some lifting of boxes may be necessary. <br>
<br>
<br>
Please review our website at www.advancedbiohealing.com for more company information.<br>
We offer a competitive benefits & compensation package!<br>
All qualified resumes should be submitted directly to careers@advancedbiohealing.com<br>
<br>
We are an Equal Opportunity Employer.<br>
]]></description>
<dc:date>2009-10-22T15:17:27-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1433376327.html</dc:source>
<dc:title><![CDATA[Quality Assurance Specialist I  (La Jolla, CA)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-22T15:17:27-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1433375161.html">
<title><![CDATA[Clinical Affairs Director (La Jolla)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1433375161.html</link>
<description><![CDATA[CLINICAL AFFAIRS DIRECTOR<br>
<br>
The West Wireless Health Institute is tax exempt research institute whose mission is to advance health and wellbeing around the world by identifying, validating and accelerating the use of innovative and cost-effective wireless solutions to critical, unmet medical and community needs.  <br>
<br>
We are currently seeking a Clinical Affairs Director who will report directly to the EVP of Medicine.  This position will be responsible for managing the planning, design, development, and implementation of strategies, plans and practices for diverse projects within the research and clinical development program at the West Wireless Health Institute.  The Clinical Affairs Manager will work as a liaison to the Institute’s outside Affiliates and also be responsible for managing the contracting and outsourcing needs of the Institute.<br>
<br>
Minimum requirements:<br>
•	Life Sciences degree, plus clinical trials contracting experience required, MBA preferred; <br>
•	A minimum of five (5) years experience in clinical research or medical device/pharmaceutical drug field and a minimum of two (2) years experience managing a professional staff;<br>
•	Working knowledge and experience of ICH-GCP guidelines, FDA and foreign regulatory requirements;<br>
•	Demonstrated study management track record showing clear proficiency in clinical project management skills and vendor management, including experience managing outsourced work;<br>
•	Ability to establish and maintain relationships with diverse organizations, agencies, and persons;<br>
•	Ability to critically review reports and prepare recommendations from such review including, but not limited to, preparing and analyzing budgets forecasts and financial reports;<br>
•	Knowledge of operational management, including budgeting; project management; broad knowledge of management principles and techniques;<br>
•	Effective interpersonal, communication (written and verbal), time management, presentation and organizational skills.<br>
<br>
Please visit our Web page for information about our company and a full description of the job at:  <br>
<a href="http://www.westwirelesshealth.org/the-institute/contact-careers.html"  rel="nofollow">http://www.westwirelesshealth.org/the-institute/contact-careers.html</a>                                                                               <br>
<br>
West Wireless Health Institute is an Equal Opportunity Employer and does not discriminate against persons on the basis of race, color, religion, national origin, sexual orientation, gender, marital status, age, disability or veteran's status.<br>
]]></description>
<dc:date>2009-10-22T15:16:24-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1433375161.html</dc:source>
<dc:title><![CDATA[Clinical Affairs Director (La Jolla)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-22T15:16:24-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/nsd/sci/1433366081.html">
<title><![CDATA[Postdoctoral Res. Assoc./Res. Sci. Intestinal Bioeng. and Biomechanics (La Jolla)]]></title>
<link>http://sandiego.craigslist.org/nsd/sci/1433366081.html</link>
<description><![CDATA[We seek a person on the postdoctoral or research scientist level to a NIH-funded project on intestinal biomechanics and motor function. The candidate must document experience with experimental work on soft tissues organs such as the digestive system or the cardiovascular system.  It is an advantage if the candidate can handle rodents. Experience in mechanical analysis will be an advantage. This is a full-time position.  Submit curriculum vitae and the names of at least three references electronically to email: hr@ljbi.org.  Reference HG-1022CL  in subject line.  LJBI offers salary commensurate with experience. Additionally, health insurance will be provided.  Further information about LJBI may be found at website: <a href="http://www.ljbi.org."  rel="nofollow">http://www.ljbi.org.</a>  LJBI is an EOE employer.<br>
]]></description>
<dc:date>2009-10-22T15:09:53-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/nsd/sci/1433366081.html</dc:source>
<dc:title><![CDATA[Postdoctoral Res. Assoc./Res. Sci. Intestinal Bioeng. and Biomechanics (La Jolla)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-22T15:09:53-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1433339936.html">
<title><![CDATA[Research Associate]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1433339936.html</link>
<description><![CDATA[BioPhase Solutions specializes in recruiting top talented professionals for San Diego's Scientific community. We are currently looking for a Research Associate to work for a leading San Diego biotechnology company.<br>
<br>
Temporary Research Associate-Biological Mass Spectrometry<br>
<br>
This position is in the Protein Biosciences department, which develops technologies for the efficient expression, purification and characterization of biotherapeutics.<br>
<br>
The primary focus will be to use mass spectrometry to assess protein drugability, protein stability, and protein identification. This requires a working knowledge of mass spectrometers and the mass spectrometry of proteins. <br>
<br>
The responsibilities include 1) Preparing protein samples for the MS 2) Operating the MS systems and data analysis tools.<br>
<br>
Experience with Waters and Agilent MS systems, Peptide alignment tools, MALDI-TOF, Monoclonal antibody analysis, and computer programming, protein purification techniques would all be considered a plus. <br>
<br>
A BS/MS degree and 3+ years of experience desired.<br>
<br>
Please also visit www.biophaseinc.com to view additional opportunities in San Diego County!<br>
]]></description>
<dc:date>2009-10-22T14:51:28-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1433339936.html</dc:source>
<dc:title><![CDATA[Research Associate]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-22T14:51:28-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1433310387.html">
<title><![CDATA[Quality Control Analyst (San Diego, CA)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1433310387.html</link>
<description><![CDATA[Pharmatek Laboratories, Inc. is a premier pharmaceutical chemistry development organization supporting the<br>
pharmaceutical and biotechnology industries. Pharmatek focuses on bringing client drug compounds from<br>
discovery to the clinic with services that include compound selection, analytical development, preformulation<br>
testing, formulation development, GMP manufacturing and stability storage and testing.<br>
Pharmatek is a team-oriented organization represented by dedicated and talented individuals. Our<br>
cross-functional teams work collaboratively in a fun, creative and satisfying environment where success is shared.<br>
We strongly believe in the development of our employees to help them achieve their professional goals and<br>
ambitions. We offer a competitive compensation and benefits package including health, dental, vision, life, long<br>
term disability coverage, and a matched 401k.<br>
<br>
Visit our website: www.pharmatek.com<br>
<br>
<br>
RESPONSIBILITIES<br>
- Maintain Quality Assurance logbooks for document change control, instrument calibration schedule, stability<br>
pull schedule, test method and technical reports, and certificates of analysis<br>
- Perform internal audits of the analytical laboratories and Quality Assurance systems as well as in-phase audits of<br>
GLP studies<br>
- Support GMP manufacturing activities including release of GMP materials, performance of line clearances in a<br>
Class 100,000 environment, maintenance of clinical trial material inventory logs<br>
- Supportive role in hosting client and regulatory audits<br>
<br>
REQUIREMENTS<br>
- BS science degree, preferably in Chemistry or Biochemistry<br>
- 1 to 2 years analytical chemistry/HPLC experience in a GMP environment required (candidates without this experience WILL NOT BE CONSIDERED)<br>
- Must be highly detail-oriented and organized<br>
- Ability to work both independently and as a team player with a positive attitude; this position requires a high<br>
level of interaction across several departments<br>
<br>
HOW TO APPLY<br>
lease apply on-line through the careers page on our website <a href="http://www.pharmatek.com/careers.html."  rel="nofollow">http://www.pharmatek.com/careers.html.</a> <br>
Once you reach this page, click on the link "current job openings"]]></description>
<dc:date>2009-10-22T14:31:17-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1433310387.html</dc:source>
<dc:title><![CDATA[Quality Control Analyst (San Diego, CA)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-22T14:31:17-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1433210309.html">
<title><![CDATA[Bio-Chemistry Assay Development  (San Diego )]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1433210309.html</link>
<description><![CDATA[Biochemistry Assay Development Consultant <br>
Contract Position <br>
<br>
<br>
Celula, Inc., a growing San Diego venture backed company, develops innovative instruments for clinical diagnostics and biomedical research using advanced micro-fluidics and other technologies. Celula identifies, develops, and validates unique cutting edge assays with significant biomedical research and clinical utility. Our devices and assays are developed to make a unique and positive impact on medical outcomes. We are looking for an experienced Bio-Chemist to join our growing and dynamic team! <br>
<br>
The Biochemistry Assay Development professional will work with an interdisciplinary team of biologists, engineers and chemists and will contribute to a variety of development projects.   This individual will conduct experiments, analyze and summarize experimental results both independently and in collaboration with other Research Associates & Scientists. <br>
<br>
Other Duties include: <br>
<br>
&#61556;	Perform PCR or similar enzymatic chemistry experiments on both commercial platforms and Celula¹s proprietary instruments.<br>
&#61556;	Test, calibrate and improve liquid handling instrumentation and processes.<br>
&#61556;	Develop SOPs for novel assays.<br>
&#61556;	Troubleshoot and improve process efficiency.<br>
&#61556;	Support additional chemistry and engineering development projects<br>
&#61556;	Other duties and projects as assigned. <br>
<br>
Qualifications:<br>
&#61556;	BS or higher in Biochemistry or chemistry required.<br>
&#61556;	Minimum 5 year’s of experience in biochemistry process/assay development required. <br>
&#61556;	Proven track record in solving complex technical issues.<br>
&#61556;	Experienced and knowledgeable in micro/nano scale liquid dispensing and handling, imaging analysis and thermal control.<br>
&#61556;	Experience and expertise in molecular assays, particularly DNA or RNA based, including fundamental knowledge and experience with reaction chemistry and optimization.<br>
&#61556;	Excellent ability to communicate and collaborate in a team environment.<br>
&#61556;	Excellent computer skills required for experiment planning, data analysis and reporting.<br>
&#61556;	Programming skills /experience required for instrument control; Labview experience is a plus.<br>
<br>
Celula, Inc. offers a competitive compensation and benefits package, including 401k and stock options. Please send resume and cover letter to: hr@celula-inc.com. <br>
See our website...www.celula-inc.com  <br>
eoe<br>
<br>
<br>
<br>
]]></description>
<dc:date>2009-10-22T13:27:04-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1433210309.html</dc:source>
<dc:title><![CDATA[Bio-Chemistry Assay Development  (San Diego )]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-22T13:27:04-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/ssd/sci/1432968781.html">
<title><![CDATA[Research/Quality Control Chemist (Carlsbad)]]></title>
<link>http://sandiego.craigslist.org/ssd/sci/1432968781.html</link>
<description><![CDATA[Research/Quality Control Chemist<br>
<br>
Take an opportunity to be part of an exciting new company and participate in the creation of new technologies.  We have a superior product on the market for the treatment of burns and we are planning to expand our product offerings.  We are looking for a chemist that can help formulate and test new products in R&D and perform with Quality Control/Quality Assurance duties.  <br>
The successful candidate will be able to design and perform experiments with limited instructions from the supervisor.  The person will have experience in the manufacture and/or testing of medical devices or pharmaceuticals. Good record keeping and attention to details are essential.<br>
Duties:<br>
•	Develop new chemical formulations for use in our product line of biosynthetic skin substitutes.<br>
•	Make R&D lab scale batches of product for evaluation.<br>
•	Perform testing on R&D product and/or coordinate testing with outside labs.<br>
•	Testing and inspection of incoming raw materials.<br>
•	Testing and inspection of manufactured goods.<br>
•	Assist all areas of the company by generating /revision documentation to FDA standards.<br>
•	Maintain training records database.<br>
•	Issue and coordinate change orders to documentation.<br>
Skills and Experience:<br>
•	Three or more years experience in Manufacturing or R&D or QC/QC in Medical Devices or Pharmaceuticals.<br>
•	Proficient in windows based computer environment including word processing, spreadsheet and database programs<br>
•	Good teamwork and interpersonal skills<br>
Education<br>
•	Bachelor’s degree from a four-year, accredited college or University<br>
Application Process: <br>
<br>
Email a cover letter including salary requirements and your résumé to info@aubreyinc.com. Candidates that do not include salary requirements will not be considered. <br>
]]></description>
<dc:date>2009-10-22T11:05:17-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/ssd/sci/1432968781.html</dc:source>
<dc:title><![CDATA[Research/Quality Control Chemist (Carlsbad)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-22T11:05:17-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1432213265.html">
<title><![CDATA[Research Associate, Analytical Chemistry (San Diego)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1432213265.html</link>
<description><![CDATA[Sapphire Energy is a venture capital backed company developing next generation biofuels based on recent advances in metabolic engineering. The company focus is the commercialization of high performance, low cost, and low carbon footprint biofuels that will substitute for conventional gasoline, diesel, and jet fuel.<br>
<br>
Key Responsibilities:<br>
The selected individual will have a solid understanding of analytical chemistry and instrumental analysis and ability to function in a highly collaborative, cross-disciplinary environment. The ideal candidate will have solid hands-on proficiency with GC, HPLC and other chromatographic techniques as well as classic sample preparation and purification techniques in order to describe and evaluate the composition of biomass and its extracts. Familiarity with spectroscopic techniques is an advantage.<br>
<br>
The selected individual will have responsibilities across a range of analytical and support activities as they relate to the functionality of lipids in algae biofuel production processes and technologies. These responsibilities will include:<br>
•Purification and characterization of biomass and extracts.<br>
<br>
•Accurate and reproducible execution of standard analytical techniques.<br>
<br>
•Providing general analytical chemistry support for project teams. <br>
<br>
•Development of  analytical methods.<br>
<br>
•Ability to effectively communicate results and interacting with project team scientists and engineers, as well as external collaboration partners.<br>
<br>
Minimum Qualifications:<br>
•Bachelor’s degree in Chemistry or Biochemistry with a minimum of 2 years of experience – industrial experience preferred.<br>
<br>
•Must be able to participate in highly effective teams. <br>
<br>
•Requires ability to use common tools for effective scientific communication within the company.<br>
<br>
•Demonstrates ability to recognize anomalous and inconsistent results and interpret experimental outcomes. <br>
<br>
Due to the collaborative nature of this position, excellent organizational, interpersonal and communications skills will be extremely important.<br>
<br>
Sapphire offers very competitive compensation packages including bonuses and equity, as well as full benefit packages which include health, dental, vision insurance, 401k, and paid time off. To apply, please send your CV and cover letter to human.resources@sapphirefuel.com.<br>
]]></description>
<dc:date>2009-10-21T19:38:49-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1432213265.html</dc:source>
<dc:title><![CDATA[Research Associate, Analytical Chemistry (San Diego)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-21T19:38:49-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1431496145.html">
<title><![CDATA[Associate Scientist III, BioPharm Sciences]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1431496145.html</link>
<description><![CDATA[BioPhase Solutions specializes in recruiting top talented professionals for San Diego's Scientific community. We are currently looking for a Associate Scientist III, BioPharm Sciences to work for a leading San Diego biotechnology company.<br>
<br>
Associate Scientist III, BioPharm Sciences<br>
<br>
Job Description:<br>
<br>
Our client is currently looking to fill a temporary Associate Scientist position in the Protein Pharmaceutical Development Department. The successful candidate will assist in device testing. This position's primary assignment will be to serve to support technical device and container closure testing. <br>
<br>
The scientist is expected to have the expertise or capability to troubleshoot (through research, observation, or laboratory testing) any and all technical design or physical issues regarding the device. <br>
<br>
Qualifications:<br>
<br>
2-4 years of industry experience with BS. 5-7 years with Technical Training Degree.<br>
<br>
Preferable Skills:<br>
<br>
-Instron Testing Machine Analyses (Design, Process, User) <br>
-Microsoft Office Proficiency (Word/Excel/Powerpoint/Project) <br>
<br>
Education <br>
<br>
BS Mechanical Engineering/BS Biomedical Engineering/BS Packaging Engineering/Technical Training Degree (Associate Degree) <br>
<br>
Please visit www.biophaseinc.com to view additional opportunities in San Diego County!]]></description>
<dc:date>2009-10-21T11:22:48-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1431496145.html</dc:source>
<dc:title><![CDATA[Associate Scientist III, BioPharm Sciences]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-21T11:22:48-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1431455254.html">
<title><![CDATA[Associate Scientist II, BioPharm Development]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1431455254.html</link>
<description><![CDATA[BioPhase Solutions specializes in recruiting top talented professionals for San Diego's Scientific community. We are currently looking for a Associate Scientist II, BioPharm Development to work for a leading San Diego biotechnology company.<br>
<br>
Associate Scientist II, BioPharm Development<br>
<br>
Job Description<br>
<br>
The successful candidate will assist in protein formulation development activities to support preclinical, clinical and commercial drug development teams. A background in biopharmaceutical formulation development is highly desirable. The candidate will be responsible for supporting protein formulation development activities, including formulation preparation, managing stability studies, analytical testing, and formulation troubleshooting. Hands-on experience in a protein biochemistry laboratory setting, spectroscopy and demonstrated technical ability with electrophoresis and protein HPLC methods are highly desired. Experience in DSC, CD and fluorescence is a plus. This position requires a detailed-oriented individual with good interpersonal and communication skills, who can work well independently and as part of a team in a dynamic, fast-moving development environment. <br>
<br>
Qualifications <br>
<br>
A BA/BS or MS in Chemistry/Biochemistry/Pharmaceutics/Chemical Engineering or related discipline with minimum of 3 years biopharmaceutical industry experience in a drug product formulations or analytical development environment is required. The candidate should have excellent laboratory, computer, documentation, communication, and organizational skills. Experience analyzing protein solutions with modern analytical methodologies (e.g. HPLC, electrophoresis, and/or spectroscopy) is also required. <br>
<br>
Education<br>
<br>
BA/BS, or MS in Chemistry/Biochemistry/Pharmaceutics /Chem. E. or related field. <br>
<br>
Please also visit www.biophaseinc.com to view additional opportunities in San Diego County!<br>
]]></description>
<dc:date>2009-10-21T11:00:13-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1431455254.html</dc:source>
<dc:title><![CDATA[Associate Scientist II, BioPharm Development]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-21T11:00:13-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1431438229.html">
<title><![CDATA[Research Associate]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1431438229.html</link>
<description><![CDATA[BioPhase Solutions specializes in recruiting top talented professionals for San Diego's Scientific community. We are currently looking for a Research Associate to work for a leading San Diego biotechnology company.<br>
<br>
Research Associate<br>
<br>
Job Description<br>
<br>
Temporary position performing purification process development. Position will perform laboratory experiments involving column chromatography, filtration, buffer making, sample submission, data analysis, and writing scientific reports. <br>
<br>
Qualifications <br>
<br>
Knowledge of column chromatography, filtration, proteins, SDS-PAGE gels, and acid-base buffers. <br>
<br>
Education<br>
<br>
BS in chemistry, engineering, or a biological science.<br>
<br>
Please also visit www.biophaseinc.com to view additional opportunities in San Diego County!<br>
]]></description>
<dc:date>2009-10-21T10:51:11-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1431438229.html</dc:source>
<dc:title><![CDATA[Research Associate]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-21T10:51:11-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1431430525.html">
<title><![CDATA[Sr. Scientist, Protein Purification]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1431430525.html</link>
<description><![CDATA[BioPhase Solutions specializes in recruiting top talented professionals for San Diego's Scientific community. We are currently looking for a Sr. Scientist, Protein Purification to work for a leading San Diego biotechnology company.<br>
<br>
Sr. Scientist, Protein Purification<br>
<br>
SUMMARY<br>
<br>
The candidate will be responsible for development of overseeing a core cohesive function in protein engineering, expression, production and characterization/validation to support the lead discovery and optimization of novel biotherapeutics across a variety of therapeutic areas. The candidate will be directly responsible for gene delivery and expression & purification of recombinant proteins from a variety of expression hosts including mammalian, E. coli, baculovirus, and yeast systems. The candidate will be responsible for designing and executing research activities that require a background in the fields of oncology, dermatology or metabolic disease in biochemistry, cell biology or related knowledge base. Additionally, the individual will be expected to contribute to and drive discovery biology efforts in a multi-disciplinary, matrix team environment. The individual must be able to function as an independent group leader with proven ability to manage a highly productive scientific staff, and will be responsible for coordinating the daily activities and training of junior scientific staff for metric and timeline driven projects. Problem troubleshooting skills and strong organizational and interpersonal skills are a must. The candidate will be responsible for preparation and dissemination of technical reports, and will be required to function in a team environment with personnel across multiple functional groups. The individual will be instrumental in the evaluation, expansion and development of new technologies that will contribute to internal technology development. <br>
<br>
PRIMARY RESPONSIBILITIES<br>
<br>
-Diverse knowledge and experience with various expression systems (E. coli, yeast, mammalian). <br>
-Experience with various expression formats (transient, stable and inducible expression). <br>
-Skilled in molecular biology techniques and their application to design of expression constructs/systems to maximize protein expression and optimize proteins for downstream uses (transient, stable and inducible expression; protein tags, chimeric molecule construction, gene delivery and targeting, etc.). <br>
-Expertise in FPLC systems and chromatographic methodologies including HIC, IEX, SEC and RP. <br>
-Experience with isolation and purification of proteins from mammalian, yeast and bacterial sources. <br>
-Knowledge and experience with expression of soluble and membrane protein targets for reagent production and support of screening efforts and target validation. <br>
-Knowledge and experience with adapting expression systems to meet project demands from high throughput protein variant screening, to larger scale demands for the support of protein characterization and pre-clinical animal studies. <br>
-Analytical techniques for the QC of protein reagents and biotherapeutics. <br>
Knowledge of protein stability and formulation methodologies is a plus.<br>
<br>
ADDITIONAL RESPONSIBILITIES<br>
<br>
-General assay development for solid-phase, solution- or cell-based assays in support of target validation. <br>
-Continuous appraisal and implementation of cutting edge technologies to provide high impact tools for discovery biology efforts (protein tags, chimeric molecule construction, gene delivery and targeting, etc.). <br>
-Ability to plan and coordinate daily activities of group personnel, interpret results and troubleshoot protocols. <br>
-Ability to comprehend pertinent literature, to work independently and meet metric-driven timelines. <br>
-Experience with surveying and generating pertinent intellectual property around technology development. <br>
-Experience with management of laboratory inventory and capital equipment purchases.<br>
<br>
EDUCATION AND EXPERIENCE<br>
<br>
-A Ph.D. or equivalent experience with 5-8 years of relevant experience in an appropriate biological descipline, with preferably 2 years of industry experience. <br>
-Ability to work in a team based environment with excellent communication skills. <br>
-Position requires routine data presentation and assembly of written research reports. <br>
-Special Training or Certification: Radioactivity and biohazard training.<br>
<br>
Please also visit www.biophaseinc.com to view additional opportunities in San Diego County!]]></description>
<dc:date>2009-10-21T10:47:12-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1431430525.html</dc:source>
<dc:title><![CDATA[Sr. Scientist, Protein Purification]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-21T10:47:12-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1430499062.html">
<title><![CDATA[Part Time / Contract Analytical Chemist (Sorrento Valley)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1430499062.html</link>
<description><![CDATA[Part Time or Contract Position in Analytical Chemistry<br>
<br>
Seeking an analytical chemist with experience in analytical and preparative use of HPLC/MS instruments, preferably in support of medicinal chemistry projects.<br>
<br>
Immediate duties include:<br>
Participate in purchase and set up of preparative HPLC equipment<br>
HPLC purification of small molecules used in drug discovery <br>
Set up new analytical methods and reports for HPLC/MS equipment <br>
Maintenance and Trouble Shooting of LC-MS Equipment<br>
Set up and maintain compound databases.<br>
Help set up and run in silico ADME prediction software <br>
Help set up and administer simple molecular modeling software <br>
Solubility assays<br>
Microsome stability assays <br>
CYP450 Inhibition assays.<br>
<br>
Requirments:<br>
BS/MS in Chemistry<br>
Three years  industry experience with analytical and preparative HPLC/MS equipment.<br>
Extensive hands on experience in troubleshooting and repair of LC/MS instruments.<br>
Ability to create and maintain databases using Excel, ISIS, and other database programs.<br>
IT and computer networking experience.<br>
Experience in conducting kinetic assays.<br>
<br>
20 hours per week, starting salary $20/hr;  Potential to move to full time.   <br>
]]></description>
<dc:date>2009-10-20T17:05:29-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1430499062.html</dc:source>
<dc:title><![CDATA[Part Time / Contract Analytical Chemist (Sorrento Valley)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-20T17:05:29-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1430442605.html">
<title><![CDATA[Salk Institute- C210 Research Assistant II/Lab Manager (La Jolla, CA)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1430442605.html</link>
<description><![CDATA[The Laboratory of Genetics, under the direction of Dr. Matthew Weitzman, is currently seeking a Research Assistant II/Lab Manager. Lab research focuses on virus-host interactions and the use of viruses as model systems to study DNA repair, signaling, cell biology, replication, innate host defenses and gene delivery. The Research Assistant II/Lab Manager is responsible for managing and supporting an active and collaborative lab group performing innovative work on virus-host interactions.
<p>
<b>Duties:</b> Technical responsibilities of the position include molecular biology techniques (cloning, PCR, DNA and RNA manipulation, Southern, Northern, and Western blotting), biochemistry (protein purification), cell biology (maintaining cells in tissue culture and transfections) and virology.
<br>
Lab management responsibilities of the position include but are not limited to: purchasing and organizing supplies and materials, and equipment maintenance. Position assists in the training of students, volunteers, and other researchers as needed. Position assists in the allocation and design of daily workflow and coordination of lab activities and is responsible for supervision of undergraduate lab assistant(s). Other administrative projects may at times be required to support the lab and may entail collaboration with other departments including but not limited to IT, HR, Research Accounting or Finance.
<p>
<b>Education:</b> Bachelor's degree in biological sciences or related field required.
<p>
<b>Experience:</b> Demonstrated experience and knowledge of molecular biology preferably in biochemistry and cell culture. Skill in the operation and maintenance of common lab equipment. Experienced with the operation of both a PC and MAC and common software applications, as well as utilizing multiple software applications for research, recording, and analysis. Demonstrated experience with general lab maintenance, including cleaning, stocking supply inventory and ensuring the maintenance of a sterile environment. Ability to manage laboratory assistants.
<p>
<b>Special Requirements:</b> The successful candidate will be highly organized, effective at multitasking, adept at juggling changing priorities and interested in becoming an integral part of the daily operation of the lab. Excellent communication skills, both oral and written are required. Strong interpersonal skills, including tact, diplomacy, and flexibility. Demonstrated ability to interact effectively with diverse groups. Must be willing to work a flexible schedule as needed to accommodate research needs. Candidates must be available for in person interviews.
<p>
<b>Physical Requirements:</b> Position requires frequent standing, sitting, repetitive hand/arm usage, carrying, bending as well as lifting and pushing up to 20lbs. Job description contains complete list of requirements.
<p>
<center><b>Interested applicants should apply online at <a href="http://www.salk.edu/careers/staff_positions.html"  rel="nofollow">http://www.salk.edu/careers/staff_positions.html</a>
]]></description>
<dc:date>2009-10-20T16:23:08-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1430442605.html</dc:source>
<dc:title><![CDATA[Salk Institute- C210 Research Assistant II/Lab Manager (La Jolla, CA)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-20T16:23:08-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1430414648.html">
<title><![CDATA[QA Supervisor/Manager]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1430414648.html</link>
<description><![CDATA[BioPhase Solutions specializes in recruiting top talented professionals for San Diego's Scientific community. We are currently looking for a QA Supervisor/Manager to work for a leading San Diego biotechnology company.<br>
<br>
QA Supervisor/Manager<br>
<br>
-Oversee the day to day activities of the QA department. <br>
-Prepares documents to send to outside centers, regulatory agencies, and for internal use. <br>
-Changes, distributes all documents, SOP’s, etc. and maintains records of documents. <br>
-Organizes and updates files in compliance with cGMP and GLP. <br>
-Reviews QC records to ensure accuracy and completeness and releases bulk peptide batches. <br>
-Schedule meetings, answer phone inquiries, distribute documents. <br>
-Technical assistance on all production & quality systems documents. <br>
-Distribute current revisions of all documents, including batch records. <br>
-Maintain calibration schedule and certificates of all production and QC equipment. <br>
-Perform internal and external audits as needed. <br>
-Assist with implementing and controlling validation program. <br>
-Generate labels for products manufactured and maintain label control to comply with regulatory requirements. <br>
-Assist with ad hoc QA projects.<br>
<br>
Please also visit www.biophaseinc.com to view additional biotech/scientific/clinical research jobs in San Diego County!]]></description>
<dc:date>2009-10-20T16:02:18-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1430414648.html</dc:source>
<dc:title><![CDATA[QA Supervisor/Manager]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-20T16:02:18-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1430342252.html">
<title><![CDATA[Research Associate (Membrane) (Sorrento Mesa)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1430342252.html</link>
<description><![CDATA[DexCom, Inc., headquartered in San Diego, California, is focused on developing technology for the continuous monitoring of glucose in people with diabetes. DexCom is committed to developing technologies and products that improve the lives of people with diabetes.  DexCom Inc. is currently seeking a Membrane Research Associate.<br>
<br>
Job Summary<br>
The Membrane Research Associate position is to be located in the Membranes materials R&D group and will be part of a small team dedicated to the support of existing product sustaining efforts and to also transition new materials and products from R&D into manufacturing.  The role will help in the creation of replacements for existing manufacturing materials and to expedite new products and materials into manufacturing.  The role will also help maintain existing product lines and continue refinements of materials and processes for cost-saving, reliability and scalability efforts.<br>
<br>
<br>
ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.<br>
•	Work on materials replacements and process revisions  <br>
<br>
•	Develop testing methodology for materials/system level testing <br>
<br>
•	Transfer new products/materials into manufacturing<br>
<br>
•	Develop and transfer new fabrication processes into manufacturing<br>
<br>
<br>
Requirements<br>
•	BS in Chemistry, Engineering, <br>
<br>
•	2+ years experience in medical devices<br>
<br>
<br>
Please send resume and salary history/requirements to: HR@dexcom.com and reference “RA Membrane” in the subject line.  <br>
<br>
DexCom offers an excellent benefits package and great work environment. For more company information, visit: www.dexcom.com <br>
<br>
<br>
]]></description>
<dc:date>2009-10-20T15:10:21-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1430342252.html</dc:source>
<dc:title><![CDATA[Research Associate (Membrane) (Sorrento Mesa)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-20T15:10:21-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1430340388.html">
<title><![CDATA[Software Test Engineer (Sorrento Mesa)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1430340388.html</link>
<description><![CDATA[DexCom, Inc., headquartered in San Diego, California, is focused on developing technology for the continuous monitoring of glucose in people with diabetes. DexCom is committed to developing technologies and products that improve the lives of people with diabetes.  DexCom Inc. is currently seeking a Software Test Engineer.<br>
<br>
Job Summary<br>
The Software Test Engineer will be responsible for software verification and validation (V&V) activities from the requirements phase through the release phase.  Software projects include the next generation of medical device, existing commercial products, Manufacturing software, and test tools.<br>
<br>
ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.<br>
<br>
•	Design, create, execute, and maintain manual and automated test cases/scripts.<br>
<br>
•	Thoroughly document test results and report test progress.<br>
<br>
•	Record and track issues in the bug tracking system.<br>
<br>
•	Analyze failures and collaborate with Software Engineers to ensure root cause is investigated.<br>
<br>
•	Create requirements traceability matrices which demonstrate test coverage of all features.<br>
<br>
•	Write test reports and obtain approvals.<br>
<br>
<br>
Requirements<br>
<br>
•	Bachelor's degree (B.S.) in Computer Science or related discipline.<br>
<br>
•	5+ years of related experience in developing test protocols and testing embedded software and software on Windows platforms.<br>
<br>
•	Automated test experience.<br>
<br>
•	Knowledge of basic C++ and scripting languages.<br>
<br>
•	Proficient in creating test plans, test cases, and test scripts.<br>
<br>
•	Excellent written and oral communication skills.<br>
<br>
•	Understanding of good software development and testing practices.<br>
<br>
<br>
•	Experience in medical device industry is a plus.<br>
<br>
Please send resume and salary history/requirements to: HR@dexcom.com and reference “Software Test Engineer” in the subject line.  <br>
<br>
DexCom offers an excellent benefits package and great work environment. For more company information, visit: www.dexcom.com <br>
<br>
]]></description>
<dc:date>2009-10-20T15:09:00-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1430340388.html</dc:source>
<dc:title><![CDATA[Software Test Engineer (Sorrento Mesa)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-20T15:09:00-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1430306899.html">
<title><![CDATA[Associate Scientist(Immuno) (Mira Mesa)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1430306899.html</link>
<description><![CDATA[Leading biotech company in Mira Mesa seeks an Associate Scientist. This position is responsible for the manufacturing and testing products in the Immunochemicals product line. Techniques include buffer preparation, SDS-PAGE, Western Blotting, ELISA, antibody purification/conjugation and mammalian cell culture. Other duties includes: vialing, packaging and general laboratory oraganization. Qualified candidate will have a B.S. or B.A. in a life science or related field and 4-6 years actual working experience. Must be proficient in the use of computers and general laboratory equipment. Experience writing and/or revising SOPs and work instructions. Overtime required. Over time required. Please submit your resume for immedidate consideration. ]]></description>
<dc:date>2009-10-20T14:46:13-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1430306899.html</dc:source>
<dc:title><![CDATA[Associate Scientist(Immuno) (Mira Mesa)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-20T14:46:13-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1430097889.html">
<title><![CDATA[Clinical Research Associate at Gen-Probe (Sorrento Mesa)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1430097889.html</link>
<description><![CDATA[<b>“The Power to Look Deeper”</b>
<br>
Awarded the 2008 Grand Prize at the local Workplace Excellence Awards, Gen-Probe is a respected biotech employer of choice in San Diego and a global leader in the research, development, manufacturing and marketing of nucleic acid probe-based products used for the diagnosis of human diseases and for screening of donated human blood.  We offer a state-of-the-art facility in a prime location with world-class benefits. We’re currently looking for team members who have “The Power to Look Deeper” in developing the best products, technologies and service.
<br>

<br>
<b>“The Power to Shape Your Future”</b>
<br>
We are seeking a mid-level (3-5 yrs experience) <b>Clinical Research Associate</b> to be assigned to high profile projects at Gen-Probe.  This full-time role will help lead the development of our clinical trial protocols and ensure adherence with GCP and company SOP’s.  
<br>

<br>
Learn more about us right by reading this recent article.  <a href="http://www3.signonsandiego.com/stories/2009/feb/22/1b22genprobe201218-diagnosis-good-gen-probe/?zIndex=56663"  rel="nofollow">http://www3.signonsandiego.com/stories/2009/feb/22/1b22genprobe201218-diagnosis-good-gen-probe/?zIndex=56663</a> 
<br>

<br>
<b>DESCRIPTION OF POSITION RESPONSIBILITIES:</b>
<br>
•Assists in the development of clinical trial protocols.
<br>
•Identifies and assists in the selection of clinical trial sites.
<br>
•Assists in the development of clinical site contracts and budgets.
<br>
•Develops clinical site training manuals and conducts site training.
<br>
•Monitors one or more clinical sites to ensure adherence to the clinical study protocol in accordance with Good Clinical Practice (GCP) and Departmental SOP’s.
<br>
•Monitors the collection and entry of study data.
<br>
•Assists in the validation and QC of clinical study database(s).
<br>

<br>
<b>RELATED BUSINESS/TECHNICAL SKILLS, KNOWLEDGE, ABILITIES:</b>
<br>
•Working knowledge of experimental and/or clinical trial design.
<br>

<br>
<b>EDUCATION AND EXPERIENCE REQUIREMENTS:</b>
<br>
•Bachelors Degree required.
<br>
•3-5 yrs experience monitoring clinical trials preferred; knowledge of diagnostic studies a plus.
<br>
•Some travel is required.
<br>

<br>
Gen-Probe offers a dynamic and innovative work environment along with excellent benefits that include sponsored medical/dental/vision benefits, stock options (NASDAQ:GPRO), bonus potential, 401(k) w/company match, paid vacation/sick time/holidays, assistance with continuing education, on-site fitness center, and our own Waterfall Café.  
<br>

<br>
We invite you to view our Career Video!
<br>
<b><a href="http://www.view-career-video.com/videos/genprobe/"  rel="nofollow">http://www.view-career-video.com/videos/genprobe/</a><b>
<br>

<br>
Please apply online by visiting:
<br>
<b><a href="http://www.gen-probe.jobs"  rel="nofollow">http://www.gen-probe.jobs</a></b> 
<br>

<br>
No agencies please.
<br>
]]></description>
<dc:date>2009-10-20T12:38:16-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1430097889.html</dc:source>
<dc:title><![CDATA[Clinical Research Associate at Gen-Probe (Sorrento Mesa)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-20T12:38:16-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1429817220.html">
<title><![CDATA[Packaging/Lab Technician (Mira Mesa)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1429817220.html</link>
<description><![CDATA[Leading biotech company in Mira Mesa has an immediate openings for an experience Packaging/Lab Technicians. The successful candidate will have 1+ years recent experience packaging at a biotech or life sciences company. This position will subdivide, label and package biochemicals using defined procedures. This includes, weighing powder and liquid material, utilizing electronic balances/scales and pipettes.  Fills appropriate containers with correct quantity and seals, labels and packages final product. <br>
Materials required may include solvents, measuring equipment, safety clothing equipment, bulk powder and liquids. Experience with SAP is a plus, along with experience in writing or revising SOPs and work instructions. Must be able to stand for extended periods and lift or move up to 50 pounds unassisted. <br>
Must have experience using: <br>
-the metric system sufficient to perform basic math calculations. <br>
-the use of electronic scales, including analytical and micro-balances, pipettes, graduated cylinders. <br>
-and solid experience in the use of computer and MS Office applications. <br>
Basic Knowledge of ISO9000 or Good Manufacturing Practices(GMP)<br>
Hours are M-F 6am -2:30 pm. Qualified candidates please submit your resume via e-mail for immediate consideration.]]></description>
<dc:date>2009-10-20T10:05:38-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1429817220.html</dc:source>
<dc:title><![CDATA[Packaging/Lab Technician (Mira Mesa)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-20T10:05:38-07:00</dcterms:issued>
</item>
<item rdf:about="http://sandiego.craigslist.org/csd/sci/1429763767.html">
<title><![CDATA[Scientific Recruiter/Internet Marketer (Sorrento Valley)]]></title>
<link>http://sandiego.craigslist.org/csd/sci/1429763767.html</link>
<description><![CDATA[Description:<br>
<br>
We are looking for an intelligent, hard working, and positive person to join our team as a Scientific Recruiter/Internet Marketer.  The position is ideal for someone that has recently graduated with a scientific degree that is eager to develop professional skills in the staffing industry.  <br>
<br>
Responsibilities:<br>
<br>
•	Source candidates from the internet, databases, and professional networks.<br>
•	Conduct phone and in person interviews daily.<br>
•	Recruit and place scientific professionals for laboratory, clinical, and executive level positions.<br>
•	Post and manage job postings and marketing material for the company across multiple divisions.<br>
•	Serve as the company’s social media guru.<br>
•	Regularly attend networking events that are scientifically and/or business related.<br>
<br>
Requirements:<br>
<br>
•	B.S. ideally in Biology, Chemistry, or any other related area.  <br>
•	Experience with social networking sites <br>
•	Experience with Microsoft Office<br>
•	Track record of high achievement, motivation, and any extracurricular accomplishments.<br>
•	Must be:<br>
- Open minded<br>
- Fast learner <br>
- Strong communicator<br>
- Challenge driven<br>
<br>
If you would like to be considered for this position, please email your resume to lsong@proveninc.com in addition to a brief cover letter which explains the following:<br>
<br>
1.	 Why are you looking for a new position?<br>
2.	List one short term goal and one long term goal.<br>
3.	What has been the biggest accomplishment of your life how it has impacted you.<br>
4.	What does resiliency mean to you?]]></description>
<dc:date>2009-10-20T09:37:46-07:00</dc:date>
<dc:language>en-us</dc:language>
<dc:rights>Copyright &#x26;copy; 2009 craigslist, inc.</dc:rights>
<dc:source>http://sandiego.craigslist.org/csd/sci/1429763767.html</dc:source>
<dc:title><![CDATA[Scientific Recruiter/Internet Marketer (Sorrento Valley)]]></dc:title>
<dc:type>text</dc:type>
<dcterms:issued>2009-10-20T09:37:46-07:00</dcterms:issued>
</item>
</rdf:RDF>