Associate Director, Analytical Development

Role: Associate Director, Analytical Development supporting mid to late-phase clinical development of Kymera's small-molecule protein degraders. Responsibilities: lead development and validation of critical analytical methods (HPLC, GC, IC, dissolution), ensure robust control strategies, review impurity characterization, design stability programs, manage external testing activities, contribute to GMP documentation, and support regulatory submissions and agency interactions. Requirements: PhD in Analytical Chemistry or related field (preferred), 10+ years in CMC analytical development of small molecules, expertise in impurity control (including PMIs and nitrosamines), extensive experience with techniques such as HPLC, GC, MS, NMR, XRPD, DSC/TGA, and dissolution, and familiarity with GLP, cGMP, and ICH standards. Preferred: experience in NDA/MAA writing, cross-functional collaboration, and regulatory interactions. HighValue: small-molecule drug development, impurity characterization, late-phase CMC, regulatory submissions, GMP stability studies, global compliance. WorkSetup: not specified.