Join Moderna as a GMP Quality Assurance Specialist at our Laval site. Ensure top-tier quality standards are met as you help bring innovative mRNA medicines to the market. In this critical role, you will provide continuous quality oversight and support the manufacturing process by ensuring compliance with GMP regulations.

This position is ideal for individuals with a passion for quality control in the pharmaceutical field and a desire to work in a dynamic environment equipped with emerging AI tools and technologies.

Key Responsibilities

- Oversee real-time quality support for manufacturing • Conduct routine facility compliance walkthroughs • Review and coordinate deviation records as needed • Author and approve quality documentation for compliance • Collaborate on internal audits and regulatory inspections Requirements:
- Bachelor’s Degree in a relevant science field • 3–5 years of experience in GMP-focused roles • Proficiency in both French and English • Adaptability to work rotating shifts • Robust understanding of GxP regulations Leverage your QA expertise at Moderna and enhance biopharmaceutical quality worldwide.

📌 GMP Quality Assurance Specialist at Moderna (Laval)
🏢 Moderna
📍 Laval