Drive quality standards in mRNA manufacturing with Moderna as a Quality Assurance Specialist at our Laval site. Engage in vital oversight to support patient-centered innovations. This role involves providing real-time quality support by monitoring manufacturing activities and ensuring compliance with established specifications.

Engage collaboratively with cross-functional teams, manage quality documentation, and support continuous enhancement efforts. Your focus on operational excellence will significantly contribute to advancing mRNA medicines for patients globally.

Key Responsibilities

- Ensure real-time Quality support on the production floor • Identify risks and gaps within GMP processes • Conduct inspections and address GMP compliance • Oversee and approve quality-related documentation • Facilitate internal audits and regulatory inspections Requirements:
- Bachelor’s Degree in science or equivalent experience • 3 – 5 years in a pharmaceutical quality role • In-depth knowledge of GxP standards • Bilingual in French and English • Available for rotating morning, afternoon, and night shifts Bring your quality expertise to Moderna and help shape the future of healthcare.

📌 Quality Assurance Specialist in Laval
🏢 BioSpace
📍 Laval