Specialist Batch Record Review | Spezi­a­list Batch Record Review (w/m/d)

Job Summary

This role involves working as a Specialist in Batch Record Review, focusing heavily on maintaining and improving Good Manufacturing Practice (GMP) compliance within a pharmaceutical production environment, specifically for Parenterals. Key responsibilities include revising and creating documentation-relevant Standard Operating Procedures (SOPs), preparing and printing batch documentation, and meticulously reviewing and processing batch records. The specialist will also support GMP audits, participate in deviation research, conduct internal training sessions, and actively drive process optimization to continuously reduce errors and improve documentation practices across various interfaces. Candidates must possess a scientific degree or relevant technical training (e.g., Pharmaceutical or Chemical Technician) and demonstrate comprehensive knowledge of GMP regulations, IT systems like MES and SAP, and strong communication skills. Fluency in German and good English skills are required for this challenging and growth-oriented position.