Become a Specialist in Validation, Commissioning, and Qualification (CQV) at the Biologics Manufacturing Centre (BMC) Inc. in Montréal. This temporary assignment emphasizes validating crucial biopharmaceutical systems and equipment. In your role, you will manage validation projects ensuring compliance with regulatory standards.

Your work will include drafting protocols, overseeing validation testing, and preparing essential documentation that contributes to the growth of Canada’s life sciences industry. Collaborating with a dedicated team, your efforts will enhance the facility's operational integrity. Key Responsibilities:
Manage validation projects for GxP compliant systems
Draft and review essential validation protocols
Execute validation testing and document results
Prepare non-conformance and validation summary reports
Support regulatory audits and change controls Requirements:
University degree in science or engineering
Minimum five years in relevant validation roles
Hands-on GMP experience and documentation skills
Bilingual: fluency in French and English
Involvement in commissioning tests and procedures Enhance biomanufacturing standards with the BMC in Montréal.

📌 Cqv Specialist At Biologics Manufacturing Centre Montreal (Canada)
🏢 Centre de production de produits biologiques
📍 Canada