Drive excellence with Moderna in Laval as a Quality Assurance specialist focused on GMP compliance. Help ensure innovative mRNA products meet the highest quality standards. This role is designed for a qualified professional with 3-5 years of experience in pharmaceutical quality assurance.

You will oversee manufacturing processes, conduct facility inspections, and implement best practices ensuring compliance with established specifications. Your ability to make informed decisions in a energetic environment will play a key role in optimizing quality operations. Key Responsibilities:

- Provide quality oversight for mRNA manufacturing
- Make informed quality decisions to prevent operational issues
- Conduct facility walkthroughs to ensure GMP standards
- Manage quality documentation and deviation records
- Support internal audits and regulatory inspections Requirements:
- Bachelor’s Degree in a science discipline
- 3-5 years in pharmaceutical quality environments
- Fluent in French and English
- Availability for rotating shifts
- Strong understanding of GxP regulations Join Moderna to make a remarkable difference in the quality of mRNA healthcare solutions.

📌 Quality Assurance Role at Moderna in Laval
🏢 Moderna Therapeutics
📍 Laval