Qa reviewer - eurofins biopharma product testing toronto, inc.
Job description
This position ensures compliance with regulations such as ISO 17025 and GMP for clients requiring quality assurance services. It involves reviewing quality documents, managing audits, and maintaining the Quality System.
Hard requirements
- Compliance with applicable regulations (ISO 17025, GMP, GLP)
- Ability to review raw laboratory data, validation studies, logbooks, and calibration reports
- Experience drafting and updating quality procedures
- Capability to assist with internal and external audits
- Knowledge of GMP and ISO 17025 standards for report accuracy
- Skill in initiating and conducting deviations, out-of-specification, and CAPA investigations
- Adherence to Standard Operating Procedures
Pay & benefits
- Competitive wages (detailed during interview)
- Health & dental coverage
- Life and disability insurance
- RRSP with 3% company match
- Paid holidays
- Paid time off
Work format
- Full-time employment type
- Location: Mississauga, ON (relocation expected in 2026)
- Start date: As soon as possible
Work location