Quality Control Analyst I - SDF

Role: Quality Control Laboratory Analyst supporting in-process, release, and stability testing of pharmaceutical products at Novo Nordisk's Durham facility. Responsibilities: perform and review analytical testing in compliance with cGMP, ensure data accuracy and environmental/GMP adherence, support deviation investigations, and facilitate transfer of technology and processes. Requirements: Bachelor's degree in chemistry or related field (or relevant experience with associate's degree or high school diploma plus extensive lab experience), minimum 1 year of lab experience, attention to detail, and ability to perform routine analytical techniques. Preferred: ability to author technical reports, troubleshoot equipment, and perform analyses such as UPLC and dissolution testing. High-value specifics: focus on oral solid dosage forms for diabetes, supporting manufacturing and quality assurance operations within a GMP environment. Collaboration: reports to Senior Manager, QC – OFP. Work setup: on-site at Durham, with physical demands including equipment handling and working with hazardous materials.