Release File Preparation Specialist Pharma | Release File Preparation Specialist Pharma (m/w/d)

Job Summary

This role involves independently compiling release documentation within the clinical study team, ensuring compliance with legal and regulatory requirements. The specialist will represent Clinical Trial Manufacturing/Release File Preparation (CTM RFP) activities and timelines, evaluate risks, and propose improvements. They will also act as a Subject Matter Expert in various improvement and innovation projects, and support internal inspections by providing documentation and presenting processes. This position requires a strong background in natural sciences, experience in GMP-regulated pharmaceutical environments, and proficiency with MS-Office and SAP systems. It's an opportunity to join an innovative pharmaceutical company, receive thorough training, and pursue professional development in a supportive team environment.