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

Job Summary

This Validation Engineer role focuses on ensuring quality and optimization within the production and packaging of sterile pharmaceuticals in Mannheim. The daily responsibilities include managing comprehensive validation and qualification processes, supporting product transfers, introducing new equipment, and optimizing existing manufacturing workflows. A key component of the role is detailed technical documentation, including creating test reports, managing deviations, and implementing change control measures. The ideal candidate holds a degree in a natural science field like Production or Mechanical Engineering and possesses sound professional experience in validation, product lifecycle management, and specific sterile production techniques such as lyophilization and filtration, coupled with strong GMP knowledge. This is a permanent, full-time opportunity offering attractive compensation and the chance to take on a key role in pharmaceutical innovation within a supportive, growth-oriented team environment.