Shape the future of biopharma with Moderna as a Quality Specialist in Laval. Monitor manufacturing quality and support compliance to uphold our high standards in medicine production. Join Moderna's Quality Assurance team and contribute to our mRNA transformation mission.

You will ensure quality oversight during manufacturing operations, collaborating closely with cross-functional teams. This role is ideal for quality professionals in a fast-paced workplace who want to facilitate continuous improvements and leverage innovative tools to enhance quality processes. Key Responsibilities:

- Monitor manufacturing activities for compliance with specifications
- Conduct facility walkthroughs to support troubleshooting
- Ensure adherence to cGMP, SOPs, and documentation
- Issue and maintain laboratory notebooks and logbooks
- Collaborate effectively on training coordination Requirements:
- Bachelor’s degree in a science discipline preferred
- 3–5 years of experience in GMP-related roles
- Demonstrated knowledge of GxP regulations
- Bilingual in French and English
- Willingness to work rotating shifts Take the next step in your quality assurance career with Moderna and make a significant impact on patient outcomes.

📌 Quality Specialist Role in Laval
🏢 Moderna
📍 Laval