Biotech QA Specialist: Batch Records & Compliance

A leading pharmaceutical company in North Carolina is seeking a Quality Assurance Specialist. This role involves performing inspections and approvals of raw materials, ensuring compliance with cGMP regulations, and reviewing manufacturing batch records. Candidates should have experience in the Pharma or Biotech industry, possess knowledge of Veeva and SAP, and hold a degree in Chemistry or Biological Sciences. Strong familiarity with FDA regulations and QA processes is essential. This position provides an opportunity to contribute significantly within a dynamic team. #J-18808-Ljbffr