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