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1. Leading and managing process engineering team (normally 5-12 members), to
ensure manufacturing process comply with medical device standards and
regulatory requirements; Take responsibility on target management, performance
review and communication, coaching and development with each team member;
帶領(lǐng)和管理工藝工程團(tuán)隊(duì)(通常5-12人), 來(lái)確保制造工藝符合醫(yī)療器械行業(yè)標(biāo)準(zhǔn)和法規(guī)要求; 負(fù)責(zé)與團(tuán)隊(duì)成員的目標(biāo)設(shè)定、績(jī)效回顧及溝通、輔導(dǎo)和發(fā)展等;
2. Take responsibility of develop key procedure/instructions/templates to be
professional and standard, to identify PDCA cycle to keep improving whole team
understanding on documents and compliance(regualations, standards, quality
system);
負(fù)責(zé)主要流程、指引、模板的專業(yè)化標(biāo)準(zhǔn)化, 制定PDCA流程以持續(xù)改善團(tuán)隊(duì)對(duì)文件的理解及合規(guī)合體系的風(fēng)險(xiǎn)考量;
3. leading team to focus on related process daily issues and problem solving,
investigating and root cause definition, correct and prevent issues by
short-term and long-term solutions;
帶領(lǐng)團(tuán)隊(duì)關(guān)于相關(guān)工藝的日常問(wèn)題解決, 調(diào)查和識(shí)別根本原因, 采取短期長(zhǎng)期措施修復(fù)和預(yù)防相關(guān)問(wèn)題;
4. leading team to focus on related manufacturing process performances
improvement through CIP tools such as lean, 6 sigma or other approach. Support
production team to secure production performance, improve efficiency and reduce
cost;
帶領(lǐng)團(tuán)隊(duì)以CIP工具（如精益、6 Sigma等）, 改進(jìn)制造工藝及技術(shù)以不斷提升制造水平. 支持生產(chǎn)團(tuán)隊(duì)確保制造水平, 提升效率, 降低成本;
5. leading team to focus on related process lifecycle management, to test and
validate new materials, new process, new technology etc.
帶領(lǐng)團(tuán)隊(duì)關(guān)注相關(guān)工藝的生命周期管理, 測(cè)試和驗(yàn)證相關(guān)新材料、新工藝、新技術(shù)等;
6. leading team to support projects, including new products introduction, new
production line build up, Automation & digitalization; to support audit from
Zeiss group, regulatory agent, Government, etc.
帶領(lǐng)團(tuán)隊(duì)支持相關(guān)項(xiàng)目包括新產(chǎn)品導(dǎo)入, 新生產(chǎn)線建立, 自動(dòng)化和數(shù)字化等; 支持來(lái)自蔡司集團(tuán)、監(jiān)管機(jī)構(gòu)、政府的審核等;
1. Minimum 5 years supervisory experience required, or young talent;
最少5年作為團(tuán)隊(duì)主管的相關(guān)經(jīng)驗(yàn), 業(yè)績(jī)優(yōu)秀或表現(xiàn)突出的人才可適當(dāng)放寬；
2. Minimum 5 years’ experience in process engineering required
最少5年工藝或制造工程類相關(guān)經(jīng)驗(yàn)；
3. Experinece in manufacturing of medical device or Pharmacy or any product in
high quality/high technology standard environment (e.g. automotive electronics,
semiconductor) is preferred
具有醫(yī)療器械制造行業(yè)或制藥或其他高質(zhì)量/高技術(shù)標(biāo)準(zhǔn)（如汽車電子，半導(dǎo)體）制造業(yè)相關(guān)工作經(jīng)驗(yàn)優(yōu)先
4. Experience of intercontinental production line transfer and process
equipment installation/validation/trouble shooting is preferred.
國(guó)際間生產(chǎn)線轉(zhuǎn)移和工藝設(shè)備安裝/驗(yàn)證/故障排除經(jīng)驗(yàn)者優(yōu)先
5.Experience in lean manufacturing, or six sigma
具備精益制造或6西格瑪經(jīng)驗(yàn)