GxP Validation Engineer & Analyst, Lab Instrumentation

Energy Jobline ZR in Cambridge seeks a Validation Specialist to support the QC Analytical department ensuring CGMP status and performing validation activities. The role entails authoring Corrective & Preventive Action plans, leading protocol deviation resolutions, and managing validation documentation. Candidates must possess validation experience in a biotech or pharmaceutical environment and a Bachelor's degree in a relevant field. Excellent knowledge of process automation, GxP compliance, and mentorship abilities are also essential. #J-18808-Ljbffr