Elevate your career with Sanofi as a GRA CMC Lead in Toronto. Focus on developing CMC regulatory strategies and engaging with global Health Authorities on vaccine projects.In this pivotal role within R&D;, you will manage project portfolios while collaborating with key stakeholders like Global Regulatory Affairs and site quality teams. Your primary duties will involve overseeing the preparation of regulatory submissions and establishing robust relationships with regulatory bodies to ensure compliance and address challenges efficiently.Key Responsibilities:
Design CMC regulatory strategies for current and marketed products
Assess Change Control processes effectively
Strengthen collaboration across CMC teams




Communicate risks and strategies for major regulatory impacts
Coordinate submission of CMC regulatory filesRequirements:
4+ years' experience in a regulatory capacity in the pharmaceuticals sector
Bachelor’s in a relevant scientific discipline
Familiarity with global regulations and Health Authority expectations
Excellent communication and problem-solving skills
Ability to foster relationships with internal and external partnersUtilize your regulatory acumen to contribute to Sanofi's mission in transforming health outcomes.#J-18808-Ljbffr

📌 Lead Cmc Regulatory Strategies At Sanofi Toronto
🏢 Biopharma Careers
📍 Toronto