Advance your career in biotech with Moderna as a Validation Specialist in Laval. Focus on commissioning, qualification, and validation in a cutting-edge GMP manufacturing setting.
As a key member of Moderna’s engineering team, you will be responsible for sustaining the validated state of GMP systems. Your role involves executing CQV activities while leveraging the latest digital technologies for validation excellence. Collaborating cross-functionally will ensure compliance with project timelines and regulatory requirements while supporting local talent development.
Key Responsibilities:
• Execute CQV activities for GMP systems and equipment
• Support validation of site facilities and utilities
• Manage requalification and maintain compliance
• Collaborate with multiple departments for validation alignment
• Author validation documentation like protocols and reports
Requirements:
• B.S. in Chemical or Mechanical Engineering
• 4–7+ years in CQV within a cGMP...