Validation Engineer | Validierungsingenieur (m/w/d)

Job Summary

This role is an exciting opportunity for a Validation Engineer to join a materials specialist focused on medical and environmental technology, operating out of a new plant established in Kleve in 2023. The core responsibilities involve ensuring compliance and quality across production processes. Day-to-day tasks include performing daily batch releases for ongoing production, validating and qualifying new production lines (IQ/OQ/PQ), and developing new customer production processes. A crucial part of the role is managing and executing all validation activities, including software validation, thermomapping, and equipment calibration. The ideal candidate will possess a degree in Bioengineering or a comparable technical field, coupled with experience in a GMP-regulated environment, preferably within Quality Management, Food, Pharma, or Medical Devices. Strong documentation skills (SOPs, validation protocols) and good written and spoken English are essential for success.