CMC Dossier Strategy Lead — Regulatory Submissions

A leading biopharmaceutical company in North Chicago seeks a Regulatory CMC Specialist to create and manage regulatory dossiers for clinical and marketing applications. The ideal candidate will have significant CMC experience, preferably with a focus on late-stage development, and strong technical writing skills. This role involves collaboration with CMC teams and serves as a subject matter expert. A comprehensive benefits package is offered, including paid time off and medical insurance. #J-18808-Ljbffr