QA Reviewer - Eurofins BioPharma Product Testing Toronto, Inc.

Added
1 day ago
Type
Full time
Salary
Salary not provided

Related skills

ms office documentation excel gmp capa

๐Ÿ“‹ Description

  • Review and determine status of quality documents (raw lab data, validation studies, logbooks
  • Support maintaining Quality System; draft/update quality procedures
  • Assist internal and external audits
  • Ensure reports and raw data comply with GMP and ISO 17025; accurate per study protocol and SOPs
  • Interact with staff to obtain information for reports and present deficiencies/improvements
  • Log and review complaints; compile ISO 17025/GMP documents for evaluation

๐ŸŽฏ Requirements

  • Knowledge of ISO 17025 and GMP requirements
  • GMP experience is an asset
  • Fluent English both written and spoken
  • Excellent communication, organizational skills, attention to detail
  • Ability to work independently and in a team; multitask and stay calm under pressure
  • Professional demeanor; maintain discretion for confidential matters

๐ŸŽ Benefits

  • Health & dental, life and disability insurance
  • RRSP with 3% company match, paid holidays, paid time off
  • Relocation: relocation to Mississauga, ON expected in 2026
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