Regulatory Affairs Specialist – FDA Submissions & CMC Expert

A pharmaceutical company is seeking a Regulatory Affairs Specialist in Bristol, TN, with expertise in oral solid dose pharmaceuticals and regulatory submissions. The role involves ensuring compliance with FDA regulations, managing submission timelines, and collaborating with cross-functional teams. Candidates should have a scientific background, with a minimum of 2 years in regulatory affairs or 4 years in the pharmaceutical industry. Familiarity with CMC and FDA submissions is highly valued. #J-18808-Ljbffr