QA Administrator - Packaging | QA-Administrator/in - Packaging (m/w/d)
TYC Personalmanagement Gerlinde Tyc
Job Summary
This QA Administrator role, focused specifically on Packaging documentation, is a crucial position within the European headquarters of a leading pharmaceutical manufacturer in Munich. The core responsibility involves ensuring regulatory compliance by meticulously reviewing batch documentation post-production and performing Quality Management (QM) releases utilizing systems like SAP/S4Hana. Daily tasks include managing controlled issuance and administration of forms, reviewing data transfers between paper and electronic systems, and preparing comprehensive batch documentation packages for internal and external audits and inspections. Candidates must have successfully completed vocational training, ideally in the pharmaceutical or related regulated industry (health/food), coupled with practical experience in QM and GMP environments. Essential requirements include strong German fluency, required English skills, and proficiency in SAP and MS Office. This role demands a reliable, meticulous, and team-oriented approach, focusing heavily on adherence to hygiene standards within the production setting.
Required Skills
Education
Successful completion of vocational training, preferably in the pharmaceutical, health, or food sector.
Experience
- Professional experience in Quality Management (QM) within an industrial production operation
- Practical experience in conducting reviews of batch documentation (electronic and paper-based)
- Experience in the pharmaceutical industry in a GMP environment (preferred)
- Experience in the health or food sector (alternative preference)
Languages
Additional
- Work predominantly in the hygiene area.
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