Description du Poste
Must Speak French!
Must have right to work in France
I’m currently supporting a pharmaceutical client who is looking to bring in an experienced QA Qualification Specialist to support a critical phase of their project.
The team is facing a documentation and QA workflow bottleneck around qualification activities, and they need additional QA bandwidth to keep timelines on track.
The Role
This is a QA-focused role, working closely with the CQV team but not a CQV execution position.
You’ll play a key role in ensuring qualification documentation is reviewed, approved, and compliant, acting as the QA interface across qualification activities.
QA review and approval of qualification protocols
Oversight of qualification-related documentation
Close collaboration with the CQV and validation teams
Ensuring documentation meets GMP and QA standards
Supporting smooth qualification workflows to avoid project delays
✅ What We’re Looking For
Strong background in Quality Assurance
Confident reviewing and approving qualification documentation
Comfortable working cross-functionally with CQV, Engineering, and QA
⚠️ You do not need to be a CQV Engineer — this role suits a QA professional who understands qualification and knows what “good” looks like from a QA perspective.
Location: On-site (details shared on discussion)
If you’re a QA professional with qualification experience and available for a fast-start contract, get in touch or apply directly.
Happy to share more details on the project and site on a call.
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Détails du Poste
Date de Publication:
March 22, 2026
Type de Poste:
Conseil
Lieu:
France
Company:
ARTO
Ready to Apply?
Don't miss this opportunity! Apply now and join our team.