Pharmaceutical Production Documentation Specialist | Mitarbeiter (gn) für die pharmazeutische Produktionsdokumentation

Job Summary

This role involves ensuring strict regulatory compliance within a global, research-oriented pharmaceutical company located in Pfaffenhofen an der Ilm. The specialist will primarily focus on post-production batch documentation, controlling data transfers, evaluating entries for completeness and plausibility, and reviewing in-process control (IPK) results against specifications. Key daily responsibilities include assessing machine and equipment documentation (e.g., protocols, process graphics), verifying input weights, balances, and yield determinations, and documenting disturbances and alarms. The specialist will also help design manufacturing protocols according to approved regulations and create comments for quality evaluation. Candidates must possess completed pharmaceutical training (e.g., Pharmaceutical Technician or Assistant) and proven experience in documentation review. Proficiency in MS Office and strong German language skills (B2 minimum) are essential. This position offers the opportunity for permanent employment and professional development in a modern, future-oriented industry.