Found Description
Support Moderna’s mission in Laval as a GMP CQV Validation Specialist, ensuring rigorous compliance in our advanced manufacturing environment. Engage in validation activities to maintain operational integrity.
In this pivotal role, you will report to the Director of Engineering & Facilities, contributing to the validated state of GMP systems. Your primary responsibilities will involve executing commissioning, qualification, and validation activities while collaborating with multiple departments to meet regulatory and quality expectations.
Key Responsibilities:
• Perform CQV activities on GMP systems and equipment
• Oversee validation of various facilities and utilities
• Manage periodic reviews and requalification processes
• Coordinate with cross-functional teams for timelines
• Author and manage validation-related documentation
Requirements:
• B.S. in Chemical or Mechanical Engineering
• 4–7+ years in CQV in a cGMP setting
• Familiarity with CAPA and ...
In this pivotal role, you will report to the Director of Engineering & Facilities, contributing to the validated state of GMP systems. Your primary responsibilities will involve executing commissioning, qualification, and validation activities while collaborating with multiple departments to meet regulatory and quality expectations.
Key Responsibilities:
• Perform CQV activities on GMP systems and equipment
• Oversee validation of various facilities and utilities
• Manage periodic reviews and requalification processes
• Coordinate with cross-functional teams for timelines
• Author and manage validation-related documentation
Requirements:
• B.S. in Chemical or Mechanical Engineering
• 4–7+ years in CQV in a cGMP setting
• Familiarity with CAPA and ...