Job title:
To be responsible for CAPA and DEFOA activities in the factory.
Your role:
Support for product quality improvement activities and to drive corrective action
Maintain the quality level to meet global quality standards
Identify opportunities and work for improvement in product quality by working closely with cross-functional team
Driving closure of assigned CAPAs in timely manner
Identify CAPA actions with CFT and track actions to close it on time
Maintain and drive CAPA and Defoa KPI
CAPA Key process to drive Improvement within the Factory, drive the CFT team to understand the Analysis tools, and drive corrective action
You’re the right fit if: (4 x bullets max)
Education Qualification: Engineering Graduate in Electronics/Telecommunication/Electrical
Work Experience:10 to 15 years of experience in Quality Assurance / Quality Control Activities in Medical devices industry preferred
Technical/Functional Competencies: Working knowledge in the following quality areas: inspection, product disposition, documentation control, Calibration and non-conforming material, and measurement system analysis. Good knowledge of the ISO13485/9001 regulations.
Behavioral Competencies: Good verbal and written influential communication skills. Good technical writing skills. Good team player and able to influence cross-functional teams
About Philips
We are a health technology company. We built our entire company around the belief that every human matters, and we won’t stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.
Learn more about our business.
Discover our rich and exciting history.
Learn more about our purpose.
If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our commitment to diversity and inclusion here.
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