Associate Director, Digital CMC & Regulatory Authoring

A leading pharmaceutical company in Topeka, KS, is seeking an Associate Principal Scientist to optimize regulatory authoring processes and enhance data management. The role involves working with cross-functional teams to develop and implement digital solutions for regulatory content, focusing on delivering increased productivity and improved data flow. Ideal candidates will have significant experience in regulatory authoring and data management within the pharmaceutical industry. #J-18808-Ljbffr