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 systemsDraft and review essential validation protocolsExecute validation testing and document resultsPrepare non-conformance and validation summary reportsSupport regulatory audits and change controlsRequirements:University degree in science or engineeringMinimum five years in relevant validation rolesHands-on GMP experience and documentation skillsBilingual: fluency in French and EnglishInvolvement in commissioning tests and proceduresEnhance biomanufacturing standards with the BMC in Montréal.

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