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

Job Summary

This specialist role focuses on ensuring regulatory compliance within a pharmaceutical environment by managing and executing crucial validation and qualification projects. Day-to-day tasks include monitoring and steering projects related to FDA/GMP standards, optimizing existing regulations in collaboration with technical and IT departments, and independently conducting internal audits. The role also involves overseeing the associated IT systems and monitoring the periodic maintenance, operation, and upkeep of machinery and equipment. Candidates must possess a completed technical or pharmaceutical technical education, coupled with several years of relevant professional experience. Success in this position requires a structured, conscientious, and team-oriented work style, along with fluent command of both German and English, making this an excellent opportunity for a detail-oriented professional seeking a permanent role in regulatory excellence.