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.
Kymera Therapeutics provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
