(Fixed Term) Specialist, Validation (CQV)

About 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 partnership with the Government of Canada strengthens pandemic preparedness by supporting rapid access to respiratory vaccines produced domestically. The mRNA vaccine manufacturing facility provides locally produced vaccines and is part of a broader effort to build a strong mRNA ecosystem in Canada.

Reporting to the Director, Engineering & Facilities, this role is central to sustaining the validated state of GMP systems across a cutting‑edge manufacturing environment.

Key Responsibilities

• Execute commissioning, qualification and validation (CQV) activities for GMP systems and equipment.
• Support validation of facilities, utilities, systems and equipment across the site.
• Execute re‑qualification a...