Senior CMC Regulatory Affairs Director

A global biopharmaceutical company based in New Jersey is seeking an Associate Director Regulatory Affairs focusing on Chemistry, Manufacturing and Controls (CMC). The role involves developing regulatory strategies, managing submissions, and liaising with regulatory agencies. The ideal candidate must have at least 8 years of pharmaceutical experience, 3 years in leadership, and a bachelor's degree in a relevant field. This position offers a comprehensive benefits package and opportunities for career development. #J-18808-Ljbffr