Associate Director, Digital CMC & Regulatory Authoring

A leading pharmaceutical company in Dover, Delaware seeks an Associate Principal Scientist, Regulatory Authoring Business Owner to optimize regulatory processes and enhance data governance. The role requires extensive knowledge in manufacturing and regulatory authoring, along with leadership in cross-functional teams. Ideal candidates will have a minimum of 8 years in the pharmaceutical industry and a strong background in project management, alongside excellent communication skills. Opportunities available for hybrid work arrangements. #J-18808-Ljbffr