Junior Specialist | Junior Specialist (m/w/d)

Job Summary

This role is ideal for a proactive Junior Specialist looking to contribute to the clinical trials supply chain within a renowned pharmaceutical company located in Biberach. Key responsibilities include supporting the processing and tracking of Out of Scope (OOS) requests, managing the processing and archiving of critical release and submission-relevant documents, and performing essential administrative duties related to the supply chain management of clinical studies. The successful candidate must possess a strong understanding of Good Manufacturing Practice (GMP) guidelines, excellent planning and organizational skills, and the ability to collaborate effectively across multidisciplinary teams. This position requires a background in natural sciences or relevant professional experience in a regulated pharmaceutical or biotechnology environment, alongside a self-reliant and responsible work ethic.