GMP Deviation Writer — QA & Root-Cause Investigator

A pharmaceutical engineering consultancy in Durham, NC, is looking for a deviation writer to join its manufacturing team. This full-time, on-site position is perfect for an early-career scientist or engineer with 1–2 years of experience in GMP manufacturing or quality support. Responsibilities include writing detailed deviation reports and collaborating with cross-functional teams to ensure compliance. The ideal candidate should possess a relevant bachelor's degree and strong analytical and writing skills. Competitive salary of $120,000.00–$125,000.00 annually offered. #J-18808-Ljbffr