Engineer, Pharmaceutical Equipment Qualification | Ingenieur (m/w/d) Anlagenqualifizierung Pharma

Job Summary

This role involves ensuring pharmaceutical manufacturing equipment meets stringent regulatory standards within the Good Manufacturing Practice (GMP) environment. The Engineer will be responsible for executing and documenting the full qualification and validation lifecycle (Installation Qualification, Operational Qualification, Design Qualification, and Performance Qualification) for pharmaceutical facilities. Day-to-day tasks include participating in Factory Acceptance Tests (FATs), creating GMP-compliant documentation, drafting Standard Operating Procedures (SOPs), and assessing the impact of technical changes. Successful candidates must hold a degree in Process Engineering, Pharmaceutical Technology, or a related field, possess strong experience in validation and qualification, and demonstrate proficiency in both German and English. This position offers the opportunity to take responsibility for complex development projects within the Life Science sector, contributing actively to team success and continuous professional growth.