Associate Director, Digital CMC & Regulatory Authoring

A global pharmaceutical company in Oklahoma City seeks an Associate Principal Scientist for Regulatory Authoring. The role involves optimizing regulatory processes and enhancing data management through digital solutions. Candidates should possess a strong background in manufacturing, regulatory authoring, and data governance, combined with 8+ years in the pharmaceutical industry. The position is part of a hybrid work model, requiring some on-site presence. #J-18808-Ljbffr