Biotechnology, Chemistry, or Biology Specialist (Clinical Documentation) | Biotechnologe (m/w/d) Chemiker (m/w/d) Biologe (m/w/d)

Job Summary

This role offers an opportunity to join a top global pharmaceutical company in Biberach, focusing on improving human life through drug development. The specialist will be responsible for managing the compilation of release documentation within the clinical study team. Key daily tasks include creating the Supply Chain Document, selecting appropriate release scenarios, ensuring timely provision of all relevant documents, and independently representing team activities and timelines within clinical study teams, adhering strictly to legal and regulatory frameworks. The role also involves risk evaluation, developing improvement suggestions, acting as a Subject Matter Expert (SME) in innovation projects, and supporting internal inspections. Candidates must possess a Master's degree in a natural science field (or a Bachelor's with extensive experience) and proven experience in GMP-regulated environments, coupled with strong communication skills in both German and English.