At a Glance
- Tasks: Manage validation projects and ensure compliance with regulatory standards in biopharmaceutical systems.
- Company: Join the Biologics Manufacturing Centre, a leader in Canada's life sciences industry.
- Benefits: Gain valuable experience in a dynamic environment with opportunities for professional growth.
- Other info: Bilingual candidates fluent in French and English are preferred.
- Why this job: Make a real impact on biomanufacturing standards while working with a dedicated team.
- Qualifications: University degree in science or engineering and five years of relevant validation experience.
The predicted salary is between 82800 - 101200 $ per year.
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 Gx P 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 in Montréal employer: Centre de production de produits biologiques Inc
Join the Biologics Manufacturing Centre in Montréal, QC, where we foster a dynamic work culture that prioritizes collaboration and innovation. As a Procurement Specialist, you'll benefit from comprehensive employee growth opportunities, competitive compensation, and a commitment to maintaining high GMP standards. Our supportive environment encourages professional development while making a meaningful impact in the biopharmaceutical industry.
Contact Details:
Centre de production de produits biologiques Inc Recruitment Team
