Job Description
The Role: Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients. Moderna is strengthening its presence in Norwood, Massachusetts, a cornerstone of our manufacturing and operational excellence. Our Norwood campus translates mRNA science into scalable impact, supporting the global delivery of our medicines. We welcome talent ready to drive innovation and make a meaningful difference for patients worldwide. In this role, you will support 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. This is a highly technical, site-based role embedded within our manufacturing ecosystem, ensuring infrastructure performance meets the highest quality and regulatory standards. Here's What You'll Do: Execute commissioning, qualification, and validation (CQV) activities for facilities, utilities, equipment, systems (FUSE), and analytical instruments. Author and execute validation lifecycle documentation including: User Requirements Specification (URS) support Risk assessments IQ/OQ/PQ protocols Summary reports Support deviation investigations, contribute to structured root cause analysis, and assist in CAPA development. Perform change control impact assessments and support implementation planning. Participate on cross-functional project teams supporting capital projects and site initiatives.