Job purpose:
· Build up and standardize the manufacturing(Machining) process
· Provide technical support on daily production operation
· Solving the problem regarding Machining process and related quality issues
Implement lean transformation, continuously improve production efficiency

Areas of responsibility:
Compliance and adherence to, at all times, applicable laws and regulations (norms) and internal Group and local and policies – particularly:
· ISO 13485
· FDA part 820 QMS
· FDA Part 11, Electronic Records; Electronic Signatures — Scope and Application
· ISO 14001
· Laws and regulations within China and those applicable to Elos Medtech Tianjin’s operations
· Elos Medtech Group’s Quality and Environmental Policies
· Elos Medtech Group Values and Our Ways
· Others as it is applicable

Functional management:
· Technical management and development in machining process.
· New product and process development and design.
· Build up and standardize the manufacturing(Machining) process
· Be responsible for Fixture & Jig designing, purchasing and maintenance, risk evaluation for process change of new tooling/equipment
· Develop, maintain and improve manufacturing documents, such as PFMEA, Procedure, SOP, WI
· Train shift leaders and operators for procedures, SOP and WI
· Provide technical support and training about Machining process
· Handle daily deviation report and lead process problem solving and root cause analysis, ensure corrective and preventive actions are taken and effective
· Support on customer complains handling and provide technical support in regards to process problem solving and root cause analysis
· Participate in NPI project as Manufacturing technical expert, lead Machining line designing/lay-out and Manufacture build
· Implement lean transformation, participate in RIE, continuously optimize manufacturing process
· Assist on production equipment maintenance and upkeep
· Implement process continuous improvement project for cost reduction and productivity increasing and quality increasing
· Promote and improve workshop 5S management

Qualifications and Desired Skills
· Bachelor degree or above, manufacturing or mechanic relevant major
· 10 years and above experience in related area of manufacturing factory with solid theoretical knowledge and practical experience & skill
· CNC working experience is must, including manually programming for CNC turning& milling compound machine (FANUC or Seimens)
· Be familiar with mechanical parts measurement technique, can choose proper tools and methodology
· Quality management capability and quality awareness is required
· AutoCAD skill required, UG modeling skill is preferred
· Experience in foreign investment enterprise is preferable
· Medical device background is preferable
· CET4, good English capability in listening, speaking and written
· 5S and lean experience is preferable
Good teamwork spirit, passion, trustworthy, result-oriented, detail oriented and able to work under pressure

醫(yī)樂世（天津）醫(yī)療器械技術(shù)有限公司，成立于2010年1月，坐落于西青開發(fā)區(qū)賽達國際工業(yè)城，是瑞典ELOS AB公司在中國投資的全資子公司，公司主要生產(chǎn)醫(yī)療器械和精密機械零部件等，擁有高精密加工工藝和嚴格的質(zhì)量控制體系。在瑞典、丹麥、美國均設有子公司。目前員工人數(shù)120人。

作為一家來自瑞典的公司，北歐的管理風格，開放的辦公環(huán)境，和諧的人文氛圍，公司不斷提高客戶滿意的同時，也在不斷完善員工各項福利。公司提供市區(qū)班車、午餐、年度健康體檢，為員工上六險一金，按照當?shù)胤ㄒ?guī)要求支付防暑降溫費、取暖費、中夜班津貼等。全員全年享有12天以上年假并逐年增加（上限20天），節(jié)日紅包、生日紅包、健康年度體檢等福利。
希望有識之士加盟，公司會為其提供良好的培訓機會及工作環(huán)境，讓我們一起開創(chuàng)美好的未來。

請詳見公司地理位置圖或使用百度地圖、谷歌地圖搜索“醫(yī)樂世”了解公司具體位置。
面試者可公交換乘708路到賽達國際工業(yè)城內(nèi)“靈北制藥站”下車，或從大寺鎮(zhèn)打車前往。