Quality Control Analyst III

Role: Laboratory Analyst in QC supporting cGMP analysis of API and finished products at Novo Nordisk's Durham facility, primarily focusing on solid dosage forms. Responsibilities: perform and review in-process, release, and stability testing, author deviations, support equipment validation, troubleshoot laboratory methods, ensure compliance with GMP and environmental standards, and drive process improvements. Requirements: Bachelor's degree or equivalent with 5+ years in pharmaceutical or clinical lab; expertise in chemistry (HPLC, UPLC, GC, etc.), microbiology, or raw materials analysis; ability to author reports; advanced knowledge of GMP; strong attention to detail. Preferred: troubleshooting skills, validation/transfer experience, project management, change control, trending. High-Value: cGMP, QC laboratory, solid dosage forms, API/stability testing, microbiology, GMP compliance, technical transfer, and process improvement in a pharmaceutical manufacturing environment. Collaboration: reports to Manager, supports other NNPILP sites, and works within cross-functional QC teams. WorkSetup: not specified; physical demands include equipment movement and work at heights, with safety considerations.