Associate Director, Digital CMC & Regulatory Authoring

A leading pharmaceutical company in Columbia, SC, is seeking an Associate Principal Scientist to enhance regulatory authoring processes. Responsibilities include defining project roadmaps, managing cross-functional teams, and developing data governance principles. The ideal candidate has extensive experience in manufacturing and regulatory authoring. This position focuses on driving innovation within a collaborative and inclusive team environment, advocating for digital transformation and efficiency in regulatory documentation practices. #J-18808-Ljbffr