GMP Support Specialist with Focus on Documentation and Complaint Management | Fachkraft (m/w/d) GMP-Support mit Schwerpunkt Dokumentations-/Reklamationsmanagement
TYC Personalmanagement Gerlinde Tyc
Job Summary
This role is for a dedicated GMP Support Specialist focusing on documentation and complaint management within a production environment for an innovative pharmaceutical company. The specialist will be responsible for managing internal packaging complaint processes, including suspected counterfeiting cases, and supporting deviation management. A key part of the role involves creating, maintaining, and optimizing Standard Operating Procedures (SOPs) and training concepts to ensure compliance with GMP and EHS guidelines. The position also requires translating overarching standards into practical departmental processes, contributing to qualification and validation activities for packaging equipment and processes, and conducting change control procedures and risk analyses. The ideal candidate will possess strong analytical skills, a high degree of quality awareness, and excellent communication abilities to collaborate effectively across interdisciplinary teams, ensuring regulatory requirements are met.
Required Skills
Education
Completed degree in Natural Sciences/Engineering or relevant vocational training with several years of practical experience
Experience
- Practical experience in a GMP-regulated environment (preferably manufacturing)
- Initial experience in creating SOPs, change control procedures, and risk analyses is desirable
Languages
Additional
- Not specified
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