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Mission: Technological support and planning of manufacturing and test processes to ensure that the setup of assembly and process will be according to our quality system and product introduction plans for medical devices 生產(chǎn)技術(shù)支持。設(shè)備，工具開發(fā)。符合質(zhì)量體系 Responsibilities: 1. Steer definition, development and implementation of production processes 掌控生產(chǎn)工藝定義, 開發(fā)和執(zhí)行 2. Transfer design from R&D to production (New project and Change Request) /研發(fā)設(shè)計導(dǎo)入(新產(chǎn)品和新修改) 3. Implement new production technologies regarding PE/應(yīng)用新的生產(chǎn)技術(shù) 4. Develop and maintain production documentation (DMR, Master plan, FMEA etc.) 開發(fā)和維護(hù)生產(chǎn)文件 5. Control the rework of failed components 掌控返修件 6. Develop and manage tooling, equipment and new technology 開發(fā)和管理生產(chǎn)工具,設(shè)備,新技術(shù)用于生產(chǎn) 7. Map for production layout (working area) 生產(chǎn)區(qū)域布局規(guī)劃 8. Participate supplier audits 參與供應(yīng)商審核 9. Support to QM to ensure that governmental and internal regulatory are followed 支持 QM 以確保符合政府和 內(nèi)部法規(guī)的要求. 10. Give PE expert knowledge input to other departments and customer 提供 PE 專家知識給其它部門或客戶 Requirements: 1. Master/Bachelor degree for science or technology education, major in Mechanical, Automation, Mechatronics Engineering, Communication, Physics, Electromagnetism etc. 理工科碩士或本科學(xué)歷，專業(yè)為機(jī)械，自動化或機(jī)電一體化，通信類，物理類，電磁類等 2. Experience in process engineering or development is preferred 工藝開發(fā)或者研發(fā)經(jīng)歷者優(yōu)先 3. Familiar with engineering tooling such as UG, Ansys etc. 熟悉工程軟件工具 4. General ability to cooperate with worldwide partners 具備與全球伙伴合作的能力