Junior GMP Specialist / Quality and Supply Chain Support - Clinical Trials | Junior GMP Specialist / Quality & Supply Chain Support (m/w/d) – Klinische Studien

Job Summary

This role involves supporting Quality Assurance and Supply Chain operations specifically within the context of clinical trials for a major pharmaceutical company. The Junior GMP Specialist will primarily focus on administrative and organizational tasks crucial for maintaining compliance. Day-to-day responsibilities include processing and tracking Out-of-Scope (OOS) requests, managing, archiving, and administering GMP-relevant documentation necessary for product release and regulatory submissions. A key function is ensuring GMP-compliant processes are followed in the manufacturing and distribution environment of clinical samples, requiring close collaboration with various internal interfaces. The ideal candidate possesses a scientific background or relevant professional experience in a GMP environment (biotechnology or pharmacy), fundamental knowledge of regulatory requirements, and strong organizational skills, coupled with proficiency in both German and English.