Associate Director, Digital CMC & Regulatory Authoring

A global pharmaceutical company is seeking an Associate Principal Scientist for the dCMC initiative in Cheyenne, Wyoming. This role focuses on optimizing regulatory authoring processes and managing digital solutions to enhance data management. Candidates should possess strong project management skills and have experience in the pharmaceutical field with an understanding of CMC operations. This position offers a hybrid work model to promote work-life balance and collaboration among diverse teams. #J-18808-Ljbffr