Validation Engineer | Validierungsingenieur (m/w/d)

Job Summary

This role involves ensuring the quality and compliance of production processes for a material specialist operating in the medical and environmental technology sectors, specifically at a new plant in Kleve, Germany. The Validation Engineer will be responsible for executing daily batch releases and leading the validation and qualification of new production lines, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ). Key duties include developing new production processes, managing all validation activities like software validation and thermal mapping, and maintaining comprehensive GMP-relevant documentation, such as SOPs and validation protocols. The ideal candidate will have a degree in Bioengineering or a comparable technical field, possess hands-on experience in a GMP-regulated environment (ideally Medical Devices or Pharma), and demonstrate strong organizational skills, supported by good written and spoken English proficiency.