GMP Manufacturing Specialist I/II — Batch Records & CAPA Lead

A leading biopharmaceutical company in North Carolina is looking for a Manufacturing Specialist I / II to provide technical support in GMP manufacturing operations. The role involves drafting manufacturing records, troubleshooting equipment, and supporting safety and compliance initiatives. Candidates should possess a High School Diploma, relevant industry experience, with degrees preferred. The position offers a full-time contract and opportunities for career growth within a global organization known for its commitment to innovation and quality. #J-18808-Ljbffr