QA Associate - Eurofins BioPharma Product Testing Toronto, Inc.
Eurofins · Toronto, Canada
QualityFull timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
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.
What they're looking for
- 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
What you'll be doing
- 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
Privacy & handoff
This role links to Eurofins's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.