GMP Validation Specialist at Moderna

Elevate your impact in biotechnology as a GMP Validation Specialist with Moderna in Laval. Focus on essential CQV activities to enhance operational readiness and compliance.
This role reports to the Director of Engineering & Facilities and is designed to sustain validated systems in a groundbreaking GMP environment. You’ll collaborate with multiple teams to ensure alignment with regulatory requirements, support deviation investigations, and participate in continuous improvement initiatives. Your expertise will play an integral role in strengthening Canada’s pandemic preparedness.
Key Responsibilities:
• Execute commissioning and qualification of GMP systems
• Document validation protocols and assessments
• Participate in internal audits and regulatory inspections
• Collaborate cross-functionally on validation deliverables
• Manage quality records related to validation activities
Requirements:
• Bachelor’s degree in Chemical or Mechanical Engineering
• 4 to...