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 GMP Support Specialist focusing on documentation and complaint management within a leading pharmaceutical company's European headquarters in Munich. The specialist will be responsible for processing complaints and suspected counterfeiting cases, managing batch documentation, coordinating inquiries, and handling change requests. A key part of the role involves creating and revising GMP documents, such as Standard Operating Procedures. The ideal candidate will possess a technical or scientific background, professional experience in the pharmaceutical industry, and strong proficiency in standard office software and SAP. This position offers an opportunity to contribute to the development and production of innovative medicines, working in a dynamic environment that values precision and teamwork.
Required Skills
Education
Completed vocational training or university degree in a technical or scientific field
Experience
- • Professional experience in the pharmaceutical industry
Languages
Additional
- Not specified
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