Quality Assurance Engineer – Batch Record Review | Ingenieur (m/w/d) Qualitätssicherung – Batch Record Review (1604)

Job Summary

This role places you at the heart of pharmaceutical production standards, where you will be responsible for ensuring GMP-compliant documentation and batch testing. Your day-to-day activities will focus on the control and release of manufacturing instructions, tracking order lead times, and managing batch documentation. You will play a vital role in audit preparation, the creation of Standard Operating Procedures (SOPs), and the implementation of new Electronic Batch Record (EBR) systems. Beyond routine checks, you will analyze production data to identify process improvements and conduct internal staff training. This position is particularly attractive for professionals seeking a long-term, permanent contract within a dynamic engineering firm, offering the chance to work on innovative pharmaceutical projects where quality and precision directly impact patient safety and product excellence.