Join Moderna's mission in Laval as a GMP Quality Assurance Specialist. Play a pivotal role in ensuring compliance and quality in mRNA manufacturing processes. In this position, you will utilize your expertise in positive manufacturing practices and collaborate with various teams to uphold exceptional quality standards.
With your background of 3-5 years in pharmaceutical quality, you will make critical decisions while monitoring real-time operations. This role also involves creating impactful quality documentation and overseeing continuous improvement initiatives. Key Responsibilities:
- Ensure compliance during all manufacturing operations
- Conduct routine facility inspections for readiness and GMP adherence
- Author and approve quality-related documentation
- Monitor quality metrics and process performance
- Lead training and development within the QA team Requirements:
- Bachelor’s Degree in a related scientific field
- 3-5 years of industry-related experience
- Proficient in French and English
- Flexibility to work various shifts
- Knowledge of GxP regulations Contribute to a culture of quality and compliance at Moderna, shaping the future of mRNA medicine.
📌 GMP Quality Assurance Specialist in Laval
🏢 Moderna Therapeutics
📍 Laval
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