職位描述
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In this role, you have the opportunity to
Maintain the quality management system compliance by ensuring the quality procedures are implemented and followed.
Supervise NPI (New Project Introduction) project, and implement design controls requirement into NPI.
Concentrate on CFR820.30 Design control and ISO13485, EU MDD/MDR, MDSAP, ISO 14971 Risk Management, IEC62304 Software development lifecycle, IEC60601, IEC62366 Usability Engineering and any other regulation/standard applied to medical device and be expert of the above regulations.
You are responsible to
Be responsible for the design control in NPI/Sustaining Project/lifecycle management Quality Assurance. (Process)
Working with these cross-functional groups, develop quality engineering documentation independently, and lead their implementation. (Process
Maintain the quality management system compliance by ensuring the quality procedures are implemented and followed.
Supervise NPI (New Project Introduction) project, and implement design controls requirement into NPI.
Concentrate on CFR820.30 Design control and ISO13485, EU MDD/MDR, MDSAP, ISO 14971 Risk Management, IEC62304 Software development lifecycle, IEC60601, IEC62366 Usability Engineering and any other regulation/standard applied to medical device and be expert of the above regulations.
You are responsible to
Be responsible for the design control in NPI/Sustaining Project/lifecycle management Quality Assurance. (Process)
Working with these cross-functional groups, develop quality engineering documentation independently, and lead their implementation. (Process
工作地點
地址:蘇州吳中區飛利浦醫療(蘇州)有限公司-中國江蘇省蘇州市工業園區鐘園路258號


職位發布者
Summ..HR
飛利浦(中國)投資有限公司

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電子技術·半導體·集成電路
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公司規模未知
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股份制企業
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田林路888號10號飛利浦上海創新科技園1號樓