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

医乐世（天津）医疗器械技术有限公司，成立于2010年1月，坐落于西青开发区赛达国际工业城，是瑞典ELOS AB公司在中国投资的全资子公司，公司主要生产医疗器械和精密机械零部件等，拥有高精密加工工艺和严格的质量控制体系。在瑞典、丹麦、美国均设有子公司。目前员工人数120人。

作为一家来自瑞典的公司，北欧的管理风格，开放的办公环境，和谐的人文氛围，公司不断提高客户满意的同时，也在不断完善员工各项福利。公司提供市区班车、午餐、年度健康体检，为员工上六险一金，按照当地法规要求支付防暑降温费、取暖费、中夜班津贴等。全员全年享有12天以上年假并逐年增加（上限20天），节日红包、生日红包、健康年度体检等福利。
希望有识之士加盟，公司会为其提供良好的培训机会及工作环境，让我们一起开创美好的未来。

请详见公司地理位置图或使用百度地图、谷歌地图搜索“医乐世”了解公司具体位置。
面试者可公交换乘708路到赛达国际工业城内“灵北制药站”下车，或从大寺镇打车前往。