GMP QC Auditor & Documentation Specialist
Eurofins is seeking a QC/Records reviewer for its Canadian operation. The role focuses on reviewing lab documents to GMP standards, ensuring data integrity in eLIMS, and supporting audits and regulatory inspections.
The successful candidate will have a 5–10 year pharma QC background, strong regulatory knowledge, and excellent communication. Relocation to Mississauga, ON is expected in 2026; the posting offers full-time benefits and career growth.
This is a great opportunity to take on the GMP QC Auditor & Documentation Specialist role at Eurofins.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the GMP QC Auditor & Documentation Specialist role in the description above.
We appreciate your interest in this position.
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