Associate Director, Digital CMC & Regulatory Authoring

A leading pharmaceutical company in Denver is seeking an Associate Principal Scientist to optimize regulatory authoring processes and enhance data management. The applicant will work with cross-functional teams to digitalize authoring, ensure governance and compliance, and drive efficiency in regulatory filings. Candidates should have significant experience in manufacturing, quality operations, and regulatory documentation. This role offers a hybrid work model. #J-18808-Ljbffr