GMP Support Qualification Specialist | Qualifizierer in der Herstellung GMP Support (m/w/d)

Job Summary

This role involves working within an interdisciplinary team at a pharmaceutical company in Idar-Oberstein to manage the qualification and validation processes during laboratory and cleanroom facility modifications. You will be responsible for the planning, execution, and documentation of re-qualifications and change-qualifications, including the validation of computer systems. A core part of your day-to-day work is ensuring that all technical equipment and facility infrastructure, such as compressed air and CO2 supply systems, remain fully compliant with current Good Manufacturing Practice (GMP) standards following site changes. The ideal candidate brings a strong technical background, a structured approach to problem-solving, and the ability to work independently in a highly regulated environment. This position offers a stable, long-term opportunity in a specialized industry with a clear path toward permanent employment, providing a high level of professional responsibility in the critical area of pharmaceutical quality assurance.