GMP Deviation Writer for Quality & CAPA

A leading engineering consultancy firm in Concord, NC is looking for a deviation writer to join their pharmaceutical manufacturing team. This full-time, on-site position is ideal for an early-career scientist or engineer with 1-2 years of experience in GMP manufacturing or quality support. The successful candidate will document investigations, collaborate with teams for root cause analysis, and contribute to continuous improvement. This role offers a supportive work environment in a dynamic industry. #J-18808-Ljbffr