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

Adecco 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…