CQV Specialist Moderna's Facility

Position: CQV Specialist for Moderna's Facility
Drive innovative mRNA solutions as a CQV Specialist at Moderna in Laval, Canada. This role centers on safeguarding compliance and optimizing validation activities for manufacturing systems.

Reporting to the Director of Engineering & Facilities, this position requires executing critical commissioning and qualification tasks to maintain high standards in our advanced manufacturing processes. Your insights will shape our validation efforts and support key regulatory inspections, ensuring all documentation is robust and precise.

Key Responsibilities:

• Execute and manage CQV activities across operations

• Author and review protocols and validation reports

• Ensure all deliverables are inspection-ready

• Support cross-functional teams on compliance matters

• Lead continuous improvement initiatives in validation processes

Requirements:

• B.S. in Chemical or Mechanical Engineering

• Minimum 4 years in CQV for cGMP facilities

• Strong skills in technical writing and collaboration

• Proven problem-solving capabilities

• Full-time position requiring on-site presence

Contribute to a commitment to excellence and change lives at Moderna.
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