Quality Management Administrator - Pharmaceutical Manufacturing | QM-Administrator/in im pharamzeutischen Umfeld (m/w/d)

Job Summary

This role is centered on ensuring the integrity and compliance of pharmaceutical production documentation for a leading global drug manufacturer based in Munich. As a Quality Management Administrator, you will be responsible for the meticulous review of data transfers between paper and electronic systems, as well as the final review of batch documentation following production. You will manage the release of quality data in SAP, oversee Work-in-Progress (WIP) reports, and handle the controlled issuance of batch documents prior to packaging. The position is ideal for professionals who thrive in highly regulated environments and possess a keen eye for detail. You will work within a collaborative team to maintain strict hygiene and GMP standards, contributing directly to the safety and quality of innovative medications. This is an excellent opportunity to join a company with a rich history in industrial drug manufacturing and a strong European presence of over 2,500 employees.