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Quality Auditor - Pharma/Cell Therapy

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SQA Services

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Location:
France , Paris ▼

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Category:
Quality Control

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Contract Type:
Not provided

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Salary:

Not provided
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Job Description:

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

Additional Information:

Job Posted:
January 02, 2026

Work Type:
On-site work
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