Enhance Canada’s biopharmaceutical capacity as a Specialist in Validation at the Biologics Manufacturing Centre in Montréal. This is a temporary position focused on validation activities for equipment and systems.

The Biologics Manufacturing

Centre is looking for a validation expert for a 12-month role in its creative biomanufacturing facility. As the Specialist in Validation, Commissioning, and Qualification, you will oversee validation projects and ensure critical compliance with industry regulations.

Your role will heavily impact the organization’s operational excellence and ability to respond to health emergencies. Key Responsibilities:

- Manage validation processes for equipment and utilities
- Execute and document validation protocols effectively




- Compile validation summary reports and assessments
- Participate in commissioning tests and audits as needed
- Draft non-conformance reports and findings Requirements:
- University degree in relevant scientific discipline
- Minimum five years’ experience in validation in the sector
- Knowledge of GMP guidelines and protocol execution
- Strong French communication skills required
- Ability to draft documentation in English Leverage your validation knowledge to support the BMC’s mission of enhancing biopharmaceutical production in Canada.

📌 Specialist in Validation and Compliance (Montreal)
🏢 Socket.dev
📍 Montreal