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

Job Summary

This role involves ensuring strict quality compliance within the manufacturing solids division of an innovative pharmaceutical company headquartered in Munich. The Quality Management Administrator will focus heavily on documentation review, including scrutinizing data transfers between paper and IT systems, and performing detailed reviews of batch documentation post-production before QM release in SAP. Key responsibilities also include managing the controlled issuance of forms and reviewing Work In Progress (WIP) reports. Candidates must possess completed vocational training, ideally in the pharmaceutical, health, or food industries, coupled with practical experience in Quality Management, particularly within a GMP-regulated industrial production environment. Strong proficiency in German and working knowledge of English, along with familiarity with SAP and MS Office, are essential for success in this detail-oriented position.