Director, CMC Regulatory Affairs - Global Drug Submissions Lead

A biotech company is seeking a Director of Regulatory Affairs, CMC to lead global regulatory strategies. The role demands over 10 years of regulatory CMC experience, including a strong understanding of scientific principles in drug development. Responsibilities include overseeing regulatory submissions and ensuring compliance with global requirements. This position requires a self-starter with excellent leadership and problem-solving abilities, capable of thriving in a fast-paced environment. Competitive salary and comprehensive benefits package are offered. #J-18808-Ljbffr