GMP Administrator QA Operations - Packaging | GMP Administrator/in (m/w/d) QA Operations - Packaging (m/w/d)

Job Summary

This role supports Quality Assurance (QA) Operations, specifically focusing on packaging documentation and Good Manufacturing Practice (GMP) compliance within a leading pharmaceutical company. The administrator will primarily manage the review and transfer of batch documentation, both paper-based and electronic, ensuring readiness for production and subsequent QA release using SAP S4/HANA. Day-to-day tasks include controlling the issuance of batch documentation before packaging, managing Work-In-Progress (WIP) protocols, and supporting the detailed planning of manufacturing orders. The ideal candidate possesses a commercial or scientific background, preferably in pharmaceuticals or related highly regulated industries (health/food), coupled with initial experience in batch documentation review. Proficiency in German (Fluent) and English (Good) is required, along with strong organizational skills and a meticulous, responsible work ethic essential for maintaining high quality standards in drug manufacturing.