GMP Documentation Specialist | GMP Documentation Specialist | M/W/D - Referenz 001091

Job Summary

This role involves supporting an internationally successful pharmaceutical company in Upper Swabia as a GMP Documentation Specialist. The primary focus is on managing and tracking Out-of-Scope (OOS) requests, ensuring meticulous processing and follow-up. Day-to-day tasks include handling and archiving documents relevant for release and submission, alongside performing administrative duties within the supply chain management for clinical trials. The ideal candidate possesses a strong understanding of GMP guidelines, excellent organizational skills, and the ability to collaborate effectively across multidisciplinary teams. This position requires a scientific background, professional experience in a GMP environment, and proficiency in both German and English, offering a chance to contribute significantly to clinical sample manufacturing processes.