Biotechnologist / Chemist / Biologist | Biotechnologe (m/w/d) Chemiker (m/w/d) Biologe (m/w/d)

Job Summary

This role offers a meaningful opportunity to contribute to the development of life-improving medications within a globally recognized pharmaceutical company in Biberach. As a key member of the clinical study team, you will be responsible for the compilation of release documentation and the creation of supply chain documents. Your day-to-day activities involve selecting appropriate release scenarios, ensuring the timely provision of all relevant documents, and representing team-related activities within clinical study teams. You will operate under strict legal and regulatory frameworks, evaluating risks and developing process improvements. Additionally, you will serve as a Subject Matter Expert (SME) in various innovation projects and support internal inspections by presenting processes and documentation. This position is particularly attractive due to its competitive compensation (approx. €68,000 p.a.), high potential for permanent takeover, and the chance to work in a top-tier GMP-regulated environment focused on professional growth and employee satisfaction.