Specialist, Quality Assurance Operations (Secondary Packaging & Clinical Trial Materials) | Specialist (m/w/d) Quality Assurance Operations Sekundärverpackung Klinikmuster
Cs2 ITEC GmbH Co. KG
Job Summary
This role is ideal for a detail-oriented professional with a scientific background seeking to ensure GxP compliance within Quality Assurance Operations, focusing specifically on secondary packaging and clinical trial materials. Day-to-day responsibilities include the critical review of batch documentation to ensure adherence to internal quality standards and GxP regulations. You will formally review and release GxP-relevant documents, such as instructions and templates, and actively support the operational departments in executing essential QA tasks, including deviation and change management. Furthermore, you will contribute to ongoing process optimization initiatives within your area and manage necessary administrative duties. The position requires strong GMP knowledge, professional experience in a regulated environment, and excellent communication skills in both German and English, offering attractive opportunities for professional growth within a supportive international team.
Required Skills
Education
Completed scientific training (e.g., Pharmaceutical Technician, Chemical Technician, Laboratory Assistant, Medical Technical Assistant, Pharmaceutical Technical Assistant)
Experience
- Professional experience in a GxP-regulated environment
- Experience applying GMP knowledge to operational QA tasks (e.g., documentation review, deviation handling)
Languages
Additional
- Not specified
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