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More info
We are looking for a Regulatory Affairs Coordinator to oversee our entire Quality program. This will be a part time permanent position (12- 16 hours per week).
Qualified candidates MUST have:
Please don’t waste either of our time if you don’t have the experience, this is NOT an entry level position.
- Prior experience controlling quality processes in an ISO 9001 or ISO 13485 environment
- Understand the issues of Medical device marketing requirements in Europe
- Experience with Microsoft and Adobe applications
- Internal and External Audit experience
- Experience with change control processes
- Experience with Competent Authorities and FDA Auditors
- Understands FDA GMP’s
- Experience developing SOP’s
We are a medical device manufacturer located in the Vista business park off of Sycamore. We have been in business for over 20 years. Please contact us if you have the experience and qualifications.
Thanks
- Location: Vista
- Compensation: $16 - $17 per hour depending on experience
- This is a part-time job.
- Principals only. Recruiters, please don't contact this job poster.
- Please, no phone calls about this job!
- Please do not contact job poster about other services, products or commercial interests.
PostingID: 1451829981