Specialist for Pharmaceutical Production Documentation | Mitarbeiter (m/w/d) für die pharmazeutische Produktionsdokumentation

Job Summary

This full-time, permanent position in Pfaffenhofen an der Ilm involves critical quality assurance and documentation control within a pharmaceutical production environment. The specialist will be responsible for reviewing batch documentation post-production, ensuring completeness, plausibility, and compliance with specifications. Key tasks include verifying data transfers (paper/electronic), checking in-process control (IPC) results, and meticulously evaluating machine, equipment, and process documentation, including protocols and process graphics, for correct process flow. Candidates must have a completed pharmaceutical education (e.g., Pharmaceutical Technician or PTA), professional experience in pharmaceutical production, and strong knowledge of GMP guidelines and drug manufacturing processes. The role requires a reliable, meticulous, and flexible approach, excellent teamwork, and good proficiency in German and MS Office tools, ideally with SAP experience.