CQV Specialist
Job in
Laval, Province de Québec, Canada
Listed on 2026-06-04
Listing for:
Moderna
Full Time
position Listed on 2026-06-04
Job specializations:
-
Engineering
Quality Engineering, Regulatory Compliance Specialist, Validation Engineer, Pharma Engineer
Job Description & How to Apply Below
Become a key player in Moderna's innovative mRNA facility in Laval as a CQV Specialist. Oversee critical validation processes that uphold the highest standards in biotechnology.
Reporting to the Director, Engineering & Facilities, this site-based position focuses on sustaining validated GMP systems.
Your role will involve executing a range of commissioning, qualification, and validation activities, working closely with various teams to ensure timely compliance and operational excellence.
Key Responsibilities:
• Lead CQV activities for systems and equipment
• Validate utilities and facilities across the site
• Engage in requalification and compliance reviews
• Collaborate with Manufacturing and Quality teams
• Prepare and review necessary validation documentation
Requirements:
• B.S. in Chemical or Mechanical Engineering
• 4–7+ years experience in cGMP validation
• Strong knowledge of CAPA and deviation management
• Excellent technical writing and collaboration skills
• Capacity to handle multiple projects
Drive validation excellence and compliance in Moderna's groundbreaking operations through your strong expertise and dedication.
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