Global CMC Regulatory Strategy Lead

A life sciences company is seeking an Associate Director, Regulatory Affairs CMC, located in San Francisco. The candidate will develop CMC regulatory strategies for products in development and post-approval, ensuring compliance with global Health Authority requirements. They will provide expertise in regulatory submissions and lead cross-functional teams. The role demands 8+ years of experience in clinical research or regulatory affairs, with a strong strategic mindset and excellent communication skills. #J-18808-Ljbffr