Validation and Qualification Specialist | ⚡⚡Validierungs- und Qualifizierungsspezialist (m/w/d)⚡

Job Summary

This critical role focuses on ensuring strict regulatory compliance for FDA/GMP-relevant products within a technical environment. The specialist is responsible for executing optimization, qualification, and validation tasks, including the monitoring and control of associated projects. Key duties involve collaborating with technical and IT departments to optimize existing regulations, conducting independent audits, and providing support for the relevant IT systems (EDV). Furthermore, the role requires oversight of the periodic maintenance, operation, and repair of essential equipment, machinery, and systems. Ideal candidates must hold an engineering degree in Pharmaceutical Technology or Mechanical Engineering, or possess comparable technical training, coupled with several years of experience in the described field. Fluency in both German and English is mandatory for successful communication and negotiation.