與今日招聘企業(yè)隨時溝通
與今日招聘企業(yè)隨時溝通
崗位職責(zé):
1. Be responsible for integrated commissioning, configuration, testing and debugging of hardware and software in the process of new product development. Also provide key technical support for marketed products and production processes.
在新產(chǎn)品開發(fā)過程中負(fù)責(zé)硬件和軟件的聯(lián)合調(diào)試、配置、測試和調(diào)試工作。同時也為上市產(chǎn)品和生產(chǎn)過程提供關(guān)鍵技術(shù)支持。
2. Develop test protocols and plans for medical devices to ensure comprehensive coverage of all functions and performance metrics. Propose testing needs, and design corresponding test cases and standards.
制定醫(yī)療設(shè)備的測試計劃和測試大綱,提出測試需求,設(shè)計相應(yīng)的測試用例和測試規(guī)范,確保測試活動全面覆蓋所有功能和性能指標(biāo)。
3. Study and implement the latest product standards and regulatory requirements, ensuring that both launched and developing products meet relevant standards and regulations.
學(xué)習(xí)并執(zhí)行最新的產(chǎn)品標(biāo)準(zhǔn)和法規(guī)要求,確保已上市產(chǎn)品和研發(fā)中的產(chǎn)品符合相關(guān)法規(guī)和產(chǎn)品技術(shù)標(biāo)準(zhǔn)要求。
4. Verify and validate the complete system, drive defect resolution, conduct tests, and produce test reports, coordinating testing activities throughout the product lifecycle.
對整機(jī)進(jìn)行驗證和確認(rèn),推動缺陷解決,執(zhí)行測試并出具測試報告,統(tǒng)籌產(chǎn)品全生命周期的測試活動。
5. Support type tests, ensuring compliance with registration requirements. Prepare and review medical device registration documentation, ensuring compliance.
支持產(chǎn)品注冊檢驗,編寫并審核醫(yī)療器械注冊資料,確保產(chǎn)品符合法規(guī)和注冊要求,確保合規(guī)性。
6. Assist in the management of the R
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