QA Compliance Auditor — GMP/ISO 17025

Eurofins; Toronto; On-site; CAD 45,000 - 55,000; Full time

Benefits offered by this job

Health & dental coverage

Life and disability insurance

RRSP with 3% company match

Paid holidays

Paid time off

Job summary

Eurofins BioPharma Product Testing Toronto, Inc. is seeking a QA Reviewer to ensure compliance with ISO 17025 and GMP. The role involves reviewing quality documents, supporting audits, and maintaining the quality system in a lab and office setting in the GTA.

The successful candidate will have a science-related degree, strong attention to detail, and excellent communication skills in English. This is a full-time position with relocation noted for 2026 within the GTA.

Qualifications

• Must have knowledge of ISO 17025 and GMP requirements.
• Fluent English with strong written and verbal communication.
• Degree or diploma in a science-related discipline is required.

Responsibilities

• Review quality documents and determine status (raw data, validation studies, logbooks).
• Assist with maintaining Quality System and update quality procedures.
• Support internal and external audits.
• Ensure reports and raw data符合 GMP and ISO 17025, per SOPs.
• Contribute to deviations, CAPA investigations, and change control.

Skills

ISO 17025

GMP compliance

Fluent English

Communication skills

Attention to detail

MS Office

Teamwork

Education

Science-related degree or diploma

Tools

MS Office

Job description

Eurofins BioPharma Product Testing Toronto, Inc. is seeking a QA Reviewer to ensure compliance with ISO 17025 and GMP. The role involves reviewing quality documents, supporting audits, and maintaining the quality system in a lab and office setting in the GTA.

The successful candidate will have a science-related degree, strong attention to detail, and excellent communication skills in English. This is a full-time position with relocation noted for 2026 within the GTA.