Associate Director, Small Molecule Drug Product & CMC

A life sciences company seeks an experienced professional to lead CMC activities for small molecule drug products. The role involves managing tech transfers and compliance with cGMP regulations, alongside overseeing CDMO facilities and ensuring successful regulatory submissions (IND, NDA, MAA). Candidates should have a relevant degree, extensive experience in project management, and the ability to work in a collaborative and fast-paced environment. Willingness to travel is a plus. #J-18808-Ljbffr