Senior Regulatory CMC Director — Global Submissions

Summit Therapeutics in Palo Alto, CA, seeks an Associate Director for Regulatory Affairs, focusing on Chemistry, Manufacturing, and Controls (CMC) to coordinate global regulatory filings. The ideal candidate will have 6+ years of experience in regulatory CMC and knowledge of FDA and EU regulations.

This hybrid role requires strong strategic input, document preparation and management of regulatory submissions. Applicants with a Bachelor's degree in Chemistry or related field and proficiency in Mandarin are highly desirable.