(Fixed Term) Specialist, Validation (CQV)

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. In Laval, Moderna’s long term partnership with the Government of Canada is strengthening the country’s pandemic preparedness. Our mRNA vaccine manufacturing facility will support rapid access to respiratory vaccines produced domestically. Through local talent development and research collaboration, we are building a strong mRNA ecosystem in Canada. Join us in shaping the future of biotechnology and healthcare innovation. Reporting to the Director, Engineering & Facilities, this role is central to sustaining the validated state of GMP systems across a cutting-edge manufacturing environment. You will execute and support Commissioning, Qualification, and Validation (CQV) activities across facilities, utilities, equipment, and processes, ensuring operational readiness and compliance. Working as an individual contributor, you will collaborate cross-functionally while leveraging digital and emerging technologies—including opportunities to engage with AI-driven validation and data integrity soluti...