GMP Documentation Specialist (m/w/d), 100%

من الإعلان الأصلي

On behalf of our client, a global leader in the **pharmaceutical industry,** we are seeking a **GMP Documentation Specialist** to support clinical biologics manufacturing operations for an **8-month project** in the Lucerne Region. In this role, you will play a key part in ensuring GMP-compliant documentation, batch record accuracy, and data integrity across manufacturing processes. Working closely with Manufacturing, Operational Excellence, and Quality teams, you will contribute to right-first-time execution and continuous improvement initiatives in a highly regulated environment.…