Job description
The Associate Director will be responsible for directing CMC analytical development initiatives, focusing on method validation and strategies for impurity management concerning small-molecule protein degraders. This role includes overseeing testing at CDMOs, managing stability programs, and aiding in regulatory submissions to ensure adherence to international standards. Applicants should have over 10 years of experience in CMC analytical development specific to small molecules and a comprehensive knowledge of cGMP and ICH guidelines. A PhD in Analytical Chemistry or a comparable life sciences discipline is highly desirable.
