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This is a contract opportunity in which you will perform 1-2 day audits at various suppliers in France. You are given the flexibility to accept or reject these assignments according to your own availability.
Job Responsibility:
Perform supplier audits at various sites within your region of residence
Assure quality in the supply chains of various clients within the pharmaceutical, medical device, cosmetics, biologics, and/or animal health industries
Coordinate, prepare, execute, and deliver supplier audits based on your own and the client schedule
Utilize your regulatory knowledge of various standards from ISO, CFR, FDA, etc
Respond to the Content team in a timely manner regarding edits/questions to your audit report
Write audit reports in accordance with client specifications
Requirements:
5+ years of hands-on audit experience in pharmaceutical, medical device, and/or biologics industries
Direct audit experience to GMP
Strong communication and writing skills
Proven ability to deescalate workplace conflicts effectively
Ability to adapt to new technology and software
Willingness to travel regionally
Nice to have:
Strong experience with 21 CFR part 1271 and cellular therapy
ISO certifications are a plus but not mandatory
What we offer:
expenses are reimbursed at cost with receipts per SQA travel policy
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