Documentation Specialist | Dokumentationsfachkraft (m/w/d)

Job Summary

As a Documentation Specialist, you will play a crucial role in ensuring the quality and compliance of pharmaceutical products by meticulously reviewing batch records for finished pharmaceuticals, bulk goods, and intermediate products. Your day-to-day responsibilities will include processing and evaluating manufacturing deviations, ensuring strict adherence to current regulations (AMG, AMWHV, GMP), and maintaining thorough documentation of all activities. You will also be responsible for reporting SOP deviations and anomalies in batch documentation, conducting training sessions in production and line clearance, and organizing GEMBA walks. This position offers an attractive opportunity within the pharmaceutical industry, providing long-term stability, competitive compensation, and comprehensive benefits.