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About this Candidate
DAVRON Report for this Quality Engineer:
- Extensive experience in medical device and pharmaceutical industries, focusing on supplier quality management and compliance with FDA guidelines and ISO standards
- Proven success in reducing incoming defect materials by 10% through effective supplier communication and audit capabilities
- Skilled in process validation and developing Production Part Approval Processes, achieving significant cost savings
- Experienced in leading cross-functional CAPA teams and utilizing statistical analysis for process improvement
- Holds a Bachelor of Science in Material Science and Engineering, Certified Quality Auditor, familiar with FDA & ISO13485 standards
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