GMP Specialist | GMP Spezialist (m/w/d)

Job Summary

This role as a GMP Specialist involves meticulous review and control of electronic manufacturing specifications (Master Batch Records) crucial for batch documentation in biopharmaceutical production, covering both Upstream and Downstream processes. Daily tasks include utilizing specialized software like BioMES 8 and SAP for master data maintenance, planning and conducting document control checks, and handling administrative duties such as processing Change Control applications, conducting internal training, and assisting with audit preparation and accompaniment. The ideal candidate holds a Bachelor’s degree in Natural Sciences or equivalent vocational training combined with significant experience in the pharmaceutical or large-scale manufacturing industry, specifically within a GMP environment. Strong IT affinity, precise working methods, and fluency in both German and English are essential for success in this permanent position.