摘要
As a QC Specialist I, you will support all GxP activities in the quality department and manage quality systems/processes including documentation, metrics, and monitoring of actions. You will also perform investigations in the quality management systems, assist in generating quality reports and GMP relevant documents.
Location : Stein
Start : asap
Duration : 12 months
About the Role
Major accountabilities:
- • OOx/deviation handling
• CAPA definition
• Ensure all activities in compliance with cGxP, incl. data integrity
• Review and approval of analytical data / tests (analytical release)
• Maintain and calibrate equipment incl. plan preparation
• Support in supplier qualification
• Trending and analysis of KPI/KQI
• Support sample planning and sampling execution
• Perform microbiological testing of materials and utilities, environmental
Minimum Requirements:
- Desirable University degree in microbiology, biochemistry, chemistry or analytical chemistry
- Collaboration, result-oriented
- Breakthrough Analysis; Being Resilient; Operational Excellence;
Continuous Learning; Digital & Tech Savvy - Laboratory equipment; Quality Control (QC) Testing; Quality Control
Sampling; Knowledge of TQM and related industry GxP standards - High level of self-awareness and responsibility in a collaborative team environment
- Very good German and English skills
Accessibility and accommodation:
Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to [email protected], and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
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