GMP Qualification Specialist - Manufacturing Support | Qualifizierer in der Herstellung GMP Support (m/w/d)
Office Events P & B GmbH
Job Summary
As a GMP Qualification Specialist in Idar-Oberstein, you will play a critical role in a pharmaceutical manufacturing environment, specifically supporting the renovation and relocation of laboratory and cleanroom facilities. Your daily responsibilities include collaborating within interdisciplinary project teams to plan, execute, and document re-qualifications and change qualifications for equipment and systems, such as compressed air and CO2 supplies. You will be responsible for ensuring all assets meet current Good Manufacturing Practice (GMP) requirements and overseeing computer system validations (CSV). This position is ideal for a detail-oriented professional with strong analytical skills who enjoys working in a highly regulated environment. The role offers an attractive salary range between €63,800 and €70,000, a structured work environment, and the opportunity for permanent takeover after an initial 18-month period, making it a stable and rewarding career move within the life sciences sector.
Required Skills
Education
University degree in Natural Sciences, Biotechnology, Process Engineering, or a comparable qualification.
Experience
- Several years of practical experience in GMP qualification, specifically involving equipment, facilities, or computer system validation.
- Professional experience in a pharmaceutical or biotechnology manufacturing environment.
- Demonstrated experience in planning and documenting re-qualifications and change qualifications.
- Proven track record of working within interdisciplinary project teams for facility upgrades or relocations.
Languages
Additional
- Location: Idar-Oberstein; Position initially limited to 18 months with an option for permanent takeover; Full-time availability required.
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