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

Job Summary

This role involves supporting a leading client in Schwäbisch Hall by overseeing critical validation and qualification tasks within a pharmaceutical production environment. As a specialist, you will be responsible for the day-to-day monitoring and management of projects related to FDA and GMP-compliant products. You will collaborate closely with Technical and IT departments to ensure all regulatory requirements are met while optimizing existing regulations. Key responsibilities include conducting independent audits, managing computer system validation (CSV), and overseeing the periodic maintenance and operation of specialized machinery and equipment. This position is particularly attractive due to its permanent contract status, competitive salary starting at €42,000 with industry surcharges, and the opportunity to work with a global market leader. It offers a structured career path with comprehensive support from the application stage through to potential permanent takeover by the client company.