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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
Vacancy posted a month ago
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