Quality Management Administrator - Manufacturing Solids | QM-Administrator/in - Manufactoring Solids (m/w/d)

Job Summary

This role involves supporting a leading pharmaceutical company in Munich with the critical quality oversight of solid drug manufacturing. As a Quality Management Administrator, you will be responsible for the day-to-day review of batch documentation, ensuring data integrity during transfers between paper and electronic systems, and managing the final QM release within SAP. You will oversee WIP reports and control the issuance of batch records prior to packaging. This position is ideal for professionals with a background in pharmaceuticals, healthcare, or food production who possess a meticulous eye for detail. It offers the unique opportunity to work within a prestigious European headquarters of a global pharmaceutical innovator, ensuring that life-saving medications meet the highest safety and regulatory standards before reaching patients.