Job Summary

• This role supports commissioning, qualification, and validation (CQV) activities to ensure facilities, utilities, equipment, systems (FUSE), and analytical instruments remain in a qualified and compliant state within a cGMP manufacturing environment.
• You will execute validation lifecycle activities, author technical documentation, and collaborate cross-functionally to maintain regulatory compliance and operational readiness.
• At Moderna, we believe that when you feel your best, you can do your best work. That’s why our US benefits and global well-being resources are designed to support you—at work, at home, and everywhere in between.

Matching Summary

Salary

Base: $74,000.00 - $118,400.00; Bonus/Equity: Eligible for annual discretionary bonus, other incentive compensation, or equity award; Benefits: Best-in-class healthcare coverage, holistic well-being resources, family planning benefits, generous paid time off, savings and investment opportunities

Skills & Requirements

Key Requirements

• B.S. in Engineering (Chemical or Mechanical preferred)
• 2–5 years of CQV or validation experience
• Working knowledge of validation lifecycle principles
• Ability to author and review technical documentation
• Structured problem-solving skills
• Strong communication skills
• Site-based role, not eligible for remote work
• Must hold work authorization in the US without future sponsorship

Work Rights