醫(yī)療器械產(chǎn)品上市后質(zhì)量監(jiān)管主管
面議
應(yīng)屆畢業(yè)生
學(xué)歷不限
- 全勤獎(jiǎng)
- 節(jié)日福利
- 不加班
- 周末雙休
職位描述
該職位還未進(jìn)行加V認(rèn)證,請(qǐng)仔細(xì)了解后再進(jìn)行投遞!
工作職責(zé)
? Responsible for Adverse Event Reporting in China
? Responsible for material hold process (own products, distributed products)
? Responsible for complaint handling and complaint investigation for medical
devices
? Responsible for Field Safety Corrective Action process in China
? Analyze safety data and advise appropriate recommendations to prevent new
or recurring incidents
? Responsible for compilation Periodic Safety Update Report for manufactured
and distributed devices
? Directly accountable for the Supplier Quality functional procedures
(Process Owner), systems, KPIs and associated process improvements to achieve
and sustain a compliant and efficient supplier management process that assures
the quality of products to our sites and customers.
? Ensures supplier and material qualifications occur according to program
timelines.
? Becomes a qualified lead auditor and performs supplier audits. Ensures
supplier audit program requirements are fulfilled.
任職要求
? Proven ability to work collaboratively
? Project management skills would be preferable.
? Strong communication and interpersonal skills with ability to work well in
high pressure environment
? Recommended 3-5 years of experience in supplier management, complaint
management or medical device manufacturing.
? Bachelor's Degree (ME, EE or equivalent)
? Direct experience within the medical device industry is preferred.
? Proven ability to demonstrate technical writing skills
? Proven knowledge in application of quality engineering
? Working experience in environments under ISO 13485
? Responsible for Adverse Event Reporting in China
? Responsible for material hold process (own products, distributed products)
? Responsible for complaint handling and complaint investigation for medical
devices
? Responsible for Field Safety Corrective Action process in China
? Analyze safety data and advise appropriate recommendations to prevent new
or recurring incidents
? Responsible for compilation Periodic Safety Update Report for manufactured
and distributed devices
? Directly accountable for the Supplier Quality functional procedures
(Process Owner), systems, KPIs and associated process improvements to achieve
and sustain a compliant and efficient supplier management process that assures
the quality of products to our sites and customers.
? Ensures supplier and material qualifications occur according to program
timelines.
? Becomes a qualified lead auditor and performs supplier audits. Ensures
supplier audit program requirements are fulfilled.
任職要求
? Proven ability to work collaboratively
? Project management skills would be preferable.
? Strong communication and interpersonal skills with ability to work well in
high pressure environment
? Recommended 3-5 years of experience in supplier management, complaint
management or medical device manufacturing.
? Bachelor's Degree (ME, EE or equivalent)
? Direct experience within the medical device industry is preferred.
? Proven ability to demonstrate technical writing skills
? Proven knowledge in application of quality engineering
? Working experience in environments under ISO 13485
工作地點(diǎn)
地址:廣州黃埔區(qū)拜耳醫(yī)藥保健
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(cái)物(如體檢費(fèi)、置裝費(fèi)、押金、服裝費(fèi)、培訓(xùn)費(fèi)、身份證、畢業(yè)證等),均涉嫌違法,請(qǐng)求職者務(wù)必提高警惕。
職位發(fā)布者
Vick..HR
拜耳醫(yī)藥保健有限公司
- 石油·石化·化工
- 200-499人
- 外商獨(dú)資·外企辦事處
- 經(jīng)濟(jì)技術(shù)開(kāi)發(fā)區(qū)
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