Pharmaceutical Production Documentation Specialist | Fachkraft für die Pharmazeutische Produktionsdokumentation (m/w/d) mit langfristiger Perspektive

Job Summary

This role involves the critical oversight and verification of batch documentation within a pharmaceutical manufacturing environment. Based in Munich at the European headquarters of an innovative pharmaceutical company, the successful candidate will ensure the integrity of production data by reviewing paper and electronic records for completeness and plausibility. Day-to-day responsibilities include checking in-process control (IPC) results, evaluating machine and equipment protocols, and verifying weighing and yield determinations. You will also play a key role in identifying deviations, assessing alarms, and supporting the design of manufacturing protocols in accordance with approved regulations. This position is ideal for detail-oriented professionals with a background in pharmacy or pharmaceutical technology who enjoy a mix of technical process evaluation and quality assurance. It offers a stable, long-term perspective with a 37.5-hour work week, primarily in a day-shift model, within a large international organization employing over 2,500 people across Europe.