Strategic Regulatory Affairs Lead - FDA Submissions

A pharmaceutical company in South Carolina is seeking a Regulatory Affairs Manager to develop regulatory strategies for ANDA submissions and ensure compliance with FDA requirements. The ideal candidate has at least 5 years of regulatory affairs experience and a Bachelor’s degree in a relevant field. Responsibilities include managing lifecycle activities, drafting technical documents, and overseeing product labeling. This role offers a dynamic work environment requiring strong problem-solving skills and teamwork. #J-18808-Ljbffr