Regulatory Documentation & Labeling Specialist (PLM/ERP)

A leading biotechnology company in North Carolina seeks a documentation expert to review, approve, and manage medical product documentation. The role requires a High School Diploma (Bachelor’s degree preferred) and 2+ years of relevant experience in a regulated industry. Key responsibilities include coordinating documentation approval processes, preparing product labeling, and ensuring compliance with regulatory guidelines. Ideal candidates should possess very good skills in Microsoft Office and exhibit strong attention to detail and organizational abilities. #J-18808-Ljbffr