GMP Documentation Specialist | GMP Documentation Specialist (m/w/d) GMP-Compliance

Job Summary

As a GMP Documentation Specialist, you will play a vital role in managing the document lifecycle for our engineering and production departments. Your day-to-day responsibilities will include creating, revising, and maintaining Standard Operating Procedures (SOPs) and forms, as well as analyzing processes to develop clear documentation. You will ensure that our document management system remains GMP-compliant, monitor document status, and prepare essential documentation packages for internal and external audits and regulatory inspections. You will serve as a key point of contact during these audits. This position is ideal for a detail-oriented professional with a background in science or technology who thrives in a collaborative, team-oriented environment. We offer a stable, long-term career path within a growing, modern family-owned pharmaceutical company, supported by professional onboarding and internal development opportunities. If you possess strong organizational skills and a commitment to quality and compliance, we invite you to join our team in Saarbrücken.