PE ME 工艺 制造工程师招聘 - 浙江巴奥米特医药产品有限公司

1.Leading and Participant into Product Transfer Projects. Ensure products successfully transferred on time and smoothly handover to production; 主导和参与到产品转移项目, 确保成功并准时的完成产品转移， 并顺利的转交到生产；
2.Developing Engineering Technical Documents, Including documents of Device Master Records(DMR), eg. DMR, BOM, Manufacturing Drawing, Manufacturing Routing, Work Instruction, CNC Program, Fixture, Tooling etc.; 开发工程技术文档，包含器械主记录的相关文档, 如DMR本身、 产品物料清单、制造图纸、制造工艺、作业指导书、CNC程序、夹具、刀具等；
3.Conduct and developing new manufacturing process and Material. Developing Process Specification and Material Specification, 导入和开发新的制造工艺。开发该工艺规范和材料规范
4.Planning and execute DOE activities, developing process validation protocol, complete validation execution with other function team, and summarize validation reports; 策划和执行DOE的相关活动，开发工艺确认方案, 与其它功能团队一起完成工艺确认的执行，并形成确认报告。
5.Leading and Participant into Continue Improvement project with Lean/6 Sigma tools and Method, intend to reduce cost, improve process and procedure, improve the product quality and production efficiency; 用Lean/六西格玛的工具和方法，主导和参与到持续改善的项目中，降低成本，改进工艺和流程，提高产品质量和生产效率；
6.Leading or Participant into CAPA and IE activities. Daily Works should comply with Regulatory Compliance Requirements 主导或参与到CAPA和IE的相关活动中， 日常工作遵循合规性的要求；
资格要求（教育、经验、知识、技能及资质等）Expected Areas of Competence (i.e., Education, experience, knowledge, skills and credentials)
1.Degree or equivalent in engineering or relevant technical discipline is prefer 工程或相关技术学科的学士学位或以上优先
2.Good written/verbal English communication skills 良好的书面/口头英语沟通技巧
3.Good interpersonal skills 良好的人际交往能力 4.Independently capable of managing tasks for multiple project plans simultaneously 同时能够独立管理多个项目的任务计划
5.Independently capable of performing logical problem solving 独立执行逻辑解决问题的能力
6.Professional and ethical conduct 职业和道德行为
7.Committed to strive for excellence in the execution of required responsibilities 致力于追求卓越在执行中所需要的责任
8 Committed to continuously learn as needed to perform the required responsibilities 致力于不断学习，需要履行必要的责任
9Learn the regulatory requirements for the Medical Device Industry 学习了解医疗行业的监管要求