Director, Regulatory CMC - Small Molecule Biotech
Kymera Therapeutics
Kymera Therapeutics is seeking a senior Regulatory Affairs CMC leader to drive global CMC strategies for degrader programs from early development through NDA/MAA submissions. You will collaborate with CMC, Quality, and Clinical teams to align regulatory plans with program timelines and ensure readiness for health authority interactions. The role emphasizes hands-on CMC submissions experience for small molecule programs, lifecycle management, and cross-functional leadership in a fast-paced #J-18808-Ljbffr Kymera Therapeutics
Vacancy posted 2 days ago
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