Position Details
Senior Regulatory Affairs Specialist (CMC/Biologics) Apply
An IT staffing company in the US is seeking a Regulatory Affairs Specialist V to author technical documents within the internal documentum system. The right candidate should have a strong scientific background, particularly in bacterial biologics, and knowledge of GMP standards relevant to clinical materials. Additionally, 3–6 years of regulatory experience in drug/biologics licensure is essential. Candidates should possess excellent writing and analytical skills and should be able to work independently under aggressive timelines. #J-18808-Ljbffr
