Validation Engineer, Sterile Pharmaceutical Production | Validierungsingenieur (m/w/d) Sterile Arzneimittelproduktion in Mannheim (1269)

Job Summary

This Validation Engineer role places you at the center of innovation and quality control within the production and packaging of sterile pharmaceuticals. Key daily responsibilities include managing and executing comprehensive validation and qualification processes, supporting product transfers, and optimizing existing manufacturing procedures and new equipment introduction. You will be responsible for meticulous documentation, including creating, managing, and archiving test reports and plans in strict adherence to regulatory standards. Furthermore, the role involves actively managing change control measures, troubleshooting deviations, and serving as a key technical consultant in interdisciplinary teams. Successful candidates must hold a scientific degree in Production Engineering, Mechanical Engineering, or a related field, coupled with fundamental experience in validation, GMP, and specific pharmaceutical production techniques such as lyophilization and filtration. This permanent, full-time position offers attractive conditions and the opportunity to drive critical process optimization in a dynamic, supportive team environment.