Advarra is seeking a consultant to provide GMP Director level support to a client in France. You will review documents being created by the GMP team prior to review by the QP. You will also assess the Quality department processes and procedures in preparation for an Audit in April 2025. (e.g., documenting CAPAs for functional areas, Site Master Validation Plan, negotiating contracts (as QAA) with service providers for facility/equipment maintenance, etc.). The site is currently only manufacturing nutritionals and derms (cosmetics).
- The position will be 30-40 hours per week starting ASAP and lasting for 6-9 months.
- Many people at the site speak English but you will interact with others that speak French. SOP’s are written in both English and French but operating instructions are only in French. This individual will need to speak French but possibly not be completely fluent.
- They prefer someone in France, however, if you are fairly close in the EU and willing to travel to their location, they will be open to consider.
If you have this type of experience please respond to by submitting your resume to: Sherr.Kollath@Advarra.com