Regulatory Affairs Specialist: CMC, NDA/ANDA Expert

A pharmaceutical organization located in Bristol, Tennessee is seeking a Regulatory Affairs Specialist. The successful candidate will support regulatory submissions and compliance activities, particularly with oral solid dose pharmaceuticals. They should have a bachelor's degree in a scientific field and at least two years of regulatory experience. Key responsibilities include preparing regulatory documents and ensuring compliance with FDA standards. Strong communication skills and a solid understanding of CMC and API change are essential for this role. #J-18808-Ljbffr