QA & Compliance Reviewer - ISO 17025/GMP

Eurofins-Canada-Biopharma; 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 regulatory compliance and accuracy of quality documents in a full-time role in Toronto.

The position emphasizes GMP and ISO 17025 adherence, with responsibilities spanning document review, quality system support, and audit assistance. The successful candidate will possess a science degree or diploma, strong English communication, and exceptional attention to detail, enabling precise report writing and data

Qualifications

• Degree or diploma in a science-related discipline.
• Excellent written and verbal English communication.
• Strong attention to detail and organizational skills.

Responsibilities

• Review and determine status of quality documents (raw data, validation studies, logbooks, calibration reports).
• Support maintenance of Quality System; draft/update quality procedures.
• Assist with internal and external audits.
• Ensure reports and raw data comply with GMP and ISO 17025; adhere to SOPs.

Skills

ISO 17025

GMP

English fluency

Communication

Attention to detail

MS Office

Organizational skills

Education

Science degree or diploma

Tools

MS Office (Excel, Word, Outlook)

Job description

Eurofins BioPharma Product Testing Toronto, Inc. is seeking a QA Reviewer to ensure regulatory compliance and accuracy of quality documents in a full-time role in Toronto.

The position emphasizes GMP and ISO 17025 adherence, with responsibilities spanning document review, quality system support, and audit assistance. The successful candidate will possess a science degree or diploma, strong English communication, and exceptional attention to detail, enabling precise report writing and data