QA Operations Administrator - Solids Manufacturing | Administrator/in (m/w/d) QA Operations - Manufacturing Solids (m/w/d)
TYC Personalmanagement Gerlinde Tyc
Job Summary
This critical role supports Quality Assurance (QA) operations within the Solids Manufacturing division of a leading pharmaceutical company. The QA Operations Administrator is responsible for ensuring compliance through meticulous handling and review of batch documentation, both electronic (using SAP 4/Hana) and paper-based. Daily tasks include reviewing data transfers, preparing and managing Work-in-Progress (WIP) protocols, and controlling the issuance of batch documentation before packaging and QA release. The position requires strong organizational skills to prepare comprehensive documentation packages for internal and external audits and inspections. Candidates must have successfully completed vocational training, ideally in the pharmaceutical or related health/food sectors, coupled with practical experience in Quality Management (QM) and Good Manufacturing Practice (GMP). This detail-oriented role requires excellent German and necessary English skills, proficiency in SAP and MS Office, and a reliable, responsible work ethic, primarily operating in a strict hygiene environment.
Required Skills
Education
Successfully completed vocational training, preferably in the pharmaceutical, health, or food industry.
Experience
- Professional experience in Quality Management (QM) within an industrial production environment
- Professional experience in the pharmaceutical industry in a GMP environment (preferred)
- Practical experience in conducting reviews of batch documentation (electronic and paper-based)
- Professional experience in the hygiene area (advantageous)
Languages
Additional
- Deployment primarily in the hygiene area.
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