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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;
帶領和管理工藝工程團隊(通常5-12人), 來確保制造工藝符合醫(yī)療器械行業(yè)標準和法規(guī)要求; 負責與團隊成員的目標設定、績效回顧及溝通、輔導和發(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);
負責主要流程、指引、模板的專業(yè)化標準化, 制定PDCA流程以持續(xù)改善團隊對文件的理解及合規(guī)合體系的風險考量;
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;
帶領團隊關(guān)于相關(guān)工藝的日常問題解決, 調(diào)查和識別根本原因, 采取短期長期措施修復和預防相關(guān)問題;
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;
帶領團隊以CIP工具（如精益、6 Sigma等）, 改進制造工藝及技術(shù)以不斷提升制造水平. 支持生產(chǎn)團隊確保制造水平, 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.
帶領團隊關(guān)注相關(guān)工藝的生命周期管理, 測試和驗證相關(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.
帶領團隊支持相關(guān)項目包括新產(chǎn)品導入, 新生產(chǎn)線建立, 自動化和數(shù)字化等; 支持來自蔡司集團、監(jiān)管機構(gòu)、政府的審核等;
1. Minimum 5 years supervisory experience required, or young talent;
最少5年作為團隊主管的相關(guān)經(jīng)驗, 業(yè)績優(yōu)秀或表現(xiàn)突出的人才可適當放寬；
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；
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)標準（如汽車電子，半導體）制造業(yè)相關(guān)工作經(jīng)驗優(yōu)先
4. Experience of intercontinental production line transfer and process
equipment installation/validation/trouble shooting is preferred.
國際間生產(chǎn)線轉(zhuǎn)移和工藝設備安裝/驗證/故障排除經(jīng)驗者優(yōu)先
5.Experience in lean manufacturing, or six sigma
具備精益制造或6西格瑪經(jīng)驗