職位描述
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In this role, you have the opportunity to
? Lead product quality issue handling in process by collaborating with production, Engineering, supplier quality engineering etc.
You are responsible for
? Plan, implement and optimize processes including design transfer, process verification and validation, engineering change etc.
? Change management to guarantee the change implementation is in compliance.
? Drive continuous improvement and CAPA culture.
? Manage nonconforming materials/Products handling procedure so that the nonconformity is handled in an appropriate way
? Carry out process/production control activities in production line, e.g. Gamba, environmental condition, ESD etc.
? Prepare the work instruction for the product release activities; train the inspectors for the product released activities;
? Kaizen event and resolution
You are a part of
?Professional Quality Engineering Team, with around 30 team peers at Shenzhen Site.
To succeed in this role, you should have the following skills and experience
1. College degree or above, major in electronics or mechanics related discipline is preferred
2. Experience: More than 3 years’ working experiences in quality functions, Experience in Medical industry and Multinational Company is preferred, Familiar with ISO 13485 and ISO 9001 quality system preferred
3. Competencies and skills:
? Strong quality knowledge like six sigma knowledge and 7 basic quality tools etc.
? Strong interpersonal communication skills
? Lean deployment experience will be an advantage
? Good English in reading and writing. CET-4 is a must or equivalent level. CET-6 is preferable
? Good knowledge in office software package (word, excel, power point, viso etc)
In return, we offer you
? Memorable working Experience in a famous MNC and Global exposure in medical industry.
? Lead product quality issue handling in process by collaborating with production, Engineering, supplier quality engineering etc.
You are responsible for
? Plan, implement and optimize processes including design transfer, process verification and validation, engineering change etc.
? Change management to guarantee the change implementation is in compliance.
? Drive continuous improvement and CAPA culture.
? Manage nonconforming materials/Products handling procedure so that the nonconformity is handled in an appropriate way
? Carry out process/production control activities in production line, e.g. Gamba, environmental condition, ESD etc.
? Prepare the work instruction for the product release activities; train the inspectors for the product released activities;
? Kaizen event and resolution
You are a part of
?Professional Quality Engineering Team, with around 30 team peers at Shenzhen Site.
To succeed in this role, you should have the following skills and experience
1. College degree or above, major in electronics or mechanics related discipline is preferred
2. Experience: More than 3 years’ working experiences in quality functions, Experience in Medical industry and Multinational Company is preferred, Familiar with ISO 13485 and ISO 9001 quality system preferred
3. Competencies and skills:
? Strong quality knowledge like six sigma knowledge and 7 basic quality tools etc.
? Strong interpersonal communication skills
? Lean deployment experience will be an advantage
? Good English in reading and writing. CET-4 is a must or equivalent level. CET-6 is preferable
? Good knowledge in office software package (word, excel, power point, viso etc)
In return, we offer you
? Memorable working Experience in a famous MNC and Global exposure in medical industry.
工作地點
地址:深圳南山區(qū)南山區(qū)科技北三路2號飛利浦大樓
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詳細位置,可以參考上方地址信息
求職提示:用人單位發(fā)布虛假招聘信息,或以任何名義向求職者收取財物(如體檢費、置裝費、押金、服裝費、培訓費、身份證、畢業(yè)證等),均涉嫌違法,請求職者務(wù)必提高警惕。
職位發(fā)布者
HR
飛利浦(中國)投資有限公司
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電子技術(shù)·半導體·集成電路
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公司規(guī)模未知
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股份制企業(yè)
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田林路888號10號飛利浦上海創(chuàng)新科技園1號樓

應屆畢業(yè)生
本科
2026-01-25 16:19:35
1779人關(guān)注
注:聯(lián)系我時,請說是在江蘇人才網(wǎng)上看到的。
