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. #J-18808-Ljbffr
CQV Specialist at Biologics Manufacturing Centre in Montréal employer: Centre de production de produits biologiques (CPPB) inc. / Biologics Manufacturing Centre (BMC) Inc.
Join a dynamic team at The Biologics Manufacturing Centre in Montréal, where we prioritise innovation and collaboration in our hybrid work environment. As a Procurement Contract Management Specialist, you'll benefit from a supportive culture that fosters professional growth and development, while playing a crucial role in shaping our sourcing strategies and supplier relationships. With a focus on GMP operations, you'll find meaningful work that directly impacts the quality of our products and services.
Contact Details:
Centre de production de produits biologiques (CPPB) inc. / Biologics Manufacturing Centre (BMC) Inc. Recruitment Team
