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

Job Summary

As a GMP Specialist, you will play a critical role in ensuring the quality and compliance of biopharmaceutical production processes. Your daily responsibilities include the GMP review of electronic Master Batch Records for both upstream and downstream production using BioMES 8 software. You will independently plan and execute the control of electronic production documentation and maintain master data within BioMES 8 and SAP. Beyond documentation, you will handle administrative tasks such as internal training, KPI tracking, onboarding new team members, managing Change Control applications, and supporting audit preparations. This role is ideal for a detail-oriented professional with a background in natural sciences or pharmaceutical manufacturing who enjoys working with complex IT systems. You will join a supportive team at a pharmaceutical company in Biberach, benefiting from a stable, long-term employment contract and a collaborative corporate culture that prioritizes professional development and equal opportunity.