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