Job Description
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 col...
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 col...