QA Associate - Eurofins BioPharma Product Testing Toronto, Inc.
Eurofins
QA Associate role providing documentation and technical support for pharmaceutical clients in a GMP environment. Responsibilities include reviewing regulatory documents, coordinating product releases, managing stability programs, and supporting compliance activities under senior supervision.
Responsibilities
- Review and reconcile GMP documents including batch records and certificates of analysis
- Coordinate product release and ensure compliance with quality standards
- Assess and trend product stability programs and manage non-conformance investigations
- Support deviation, CAPA, and change control evaluations and documentation
- Assist with inspections, audits, and client SOP training and maintenance
Requirements
- 1-2 years experience in GMP environment
- Bachelor's degree in Chemistry, Microbiology, or Biochemistry; or related diploma
- Solid understanding of chemistry and microbiology fundamentals
- Microsoft Office proficiency, particularly Excel
- Fluent French communication skills, verbal and written
- Willingness to travel within Canada for business purposes
- Pharmaceutical, Natural Health Products, or Medical Devices experience preferred
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