GMP QA Intern — Documentation & Records
Listed on 2026-10-11
-
Quality Assurance - QA/QC
QA Specialist - Analyst/Manager, Regulatory Compliance Specialist -
Pharmaceutical
Regulatory Compliance Specialist
Moderna Laval internships in Quality Assurance are full-time positions based in Laval, Canada from May to August 2027. The intern will support Quality operations and Quality Systems activities at Moderna’s cGMP facility, gaining exposure to GMP, controlled documentation, training administration, records management, and quality-system support in a regulated biopharma environment.
The role emphasizes documentation accuracy, inspection readiness, and collaboration with cross-functional teams, while
This role, GMP QA Intern — Documentation & Records at Moderna Therapeutics, could be your next opportunity.
Learn more about the GMP QA Intern — Documentation & Records role in the description above.
We appreciate your interest in this position.
Join Moderna Therapeutics and contribute to our ongoing work.
Take a moment to read everything above and see whether this role is right for you.
This posting is for the GMP QA Intern — Documentation & Records role at Moderna Therapeutics, based in Laval (administrative region), QC, Canada.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).