Quality Control Analyst II - SDF

Role: QC Analyst in pharmaceutical manufacturing at Novo Nordisk's Durham facility, focusing on analysis of in-process, release, and stability samples for oral treatments for type 2 diabetes. Responsibilities include conducting laboratory tests in compliance with cGMP, authoring deviation reports, supporting system validations, and ensuring data accuracy and environmental/GMP compliance. The role involves maintaining testing proficiency, troubleshooting laboratory equipment, and supporting change control activities. Requirements: Bachelor’s degree in Chemistry or relevant field, with a minimum of 3 years' experience in a clinical or industrial/pharmaceutical lab; associate’s or high school diploma with equivalent experience also considered. Preferred skills include GMP knowledge, technical report writing, troubleshooting, and experience with tablet analysis techniques such as UPLC and dissolution. The position reports to the Senior Manager, QC, and involves adherence to safety protocols. Work setup is on-site in Durham, NC, with physical requirements including handling equipment up to 33 pounds, working at heights occasionally, and performing precise manual tasks.