Associate Director, Digital CMC & Regulatory Authoring

A global pharmaceutical company is looking for an Associate Principal Scientist to optimize regulatory authoring processes and enhance data management. This position involves working with a cross-functional team to define and implement a digital solution for regulatory filing sections. The ideal candidate should have extensive knowledge of manufacturing processes, regulatory authoring experience, and a strong understanding of data management initiatives. This role offers a hybrid working model in Montgomery, Alabama. #J-18808-Ljbffr