Associate Director, Digital CMC & Regulatory Authoring

A leading global pharmaceutical company is seeking an Associate Principal Scientist, Regulatory Authoring Business Owner to lead the optimization of regulatory authoring processes. This role involves collaborating with various stakeholders to develop digital solutions for regulatory submission, enhancing data management practices, and providing oversight for user adoption and testing. Ideal candidates will have a strong background in regulatory authoring and experience in project management within the pharmaceutical industry. #J-18808-Ljbffr