QA/QM Operations Administrator - Manufacturing Solids | QM-Administrator/in - Manufactoring Solids (m/w/d)

Job Summary

This role requires a diligent QA/QM Operations Administrator to ensure the quality and compliance of solid manufacturing processes for an innovative pharmaceutical leader based near Munich. Day-to-day responsibilities focus heavily on documentation control, including the meticulous review of data transfers between paper and electronic systems, and the preparation and final review of batch documentation both before production start and prior to QA release within SAP 4/Hana. You will also manage Work-In-Progress (WIP) protocols, control the issuance of documentation before packaging, and prepare comprehensive batch documentation necessary for internal audits and external inspections. The ideal candidate has successfully completed vocational training, preferably in the pharmaceutical or related health/food sectors, and possesses professional experience in Quality Management within a GMP-regulated industrial production setting. Strong practical experience in reviewing complex batch records and fluent German skills are essential, alongside proficiency in SAP and MS Office.