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

Job Summary

This full-time role in Pfaffenhofen an der Ilm involves the critical oversight of pharmaceutical manufacturing records. Day-to-day, you will be responsible for reviewing batch documentation for completeness and plausibility, verifying in-process control (IPC) results, and evaluating machine and process logs to ensure compliance with production standards. You will play a key role in assessing malfunctions, alarms, and quality-relevant diagnoses, while also assisting in the creation of manufacturing protocols according to approved regulations. This position is ideal for detail-oriented professionals with a background in pharmacy or pharmaceutical manufacturing who enjoy ensuring regulatory compliance (GMP). The role offers a permanent contract with above-tariff remuneration, holiday and Christmas bonuses, and a strong perspective for permanent takeover by the client company, making it an excellent opportunity for long-term career stability in the pharmaceutical industry.