A
GMP Documentation Specialist (m/w/d), 100%
Adecco
On-site
From the original posting
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.…
Excerpt from the original posting (German). Full details are on the employer site.m3rad Jobs does not hire and does not represent the employer. The original posting is the reference.