FDA-GLP, GCP, and TPD knowledge anchors this quality-focused position at Altasciences. Conduct audits, address QA citations, and protect documentation accuracy.

As a Quality Control Reviewer, you perform comprehensive documentation review for the Sample Management team and support its quality requirements. You develop, execute, and report audits, complete information forms, and track deviations or non-conformance reports. The position also involves responding to QA citations and keeping current with regulatory developments, SOPs, procedures, and techniques through training, meetings, and internal communications.

Key Responsibilities:

- Review all documentation generated by Sample Management
- Perform team audits and prepare written reports
- Complete forms supporting accurate,



complete documentation
- Document deviations and non-conformance reports
- Monitor regulatory developments and respond to QA citations

Requirements:

- At least three years’ experience with relevant diploma or equivalent
- In-depth FDA-GLP, GCP, and TPD knowledge
- Detail-oriented, customer-oriented approach
- Robust leadership, decision-making, and problem-solving skills
- Bilingual French and English communication

Bring regulatory knowledge, audit execution, and detail-oriented judgment to quality control review within Altasciences’ Sample Management team.

📌 GLP GCP Quality Assurance Auditor (Laval)
🏢 Altasciences
📍 Laval