Engineer - Manufacturing Support

About the role

Cochlear is the global market leader in implant hearing solutions. Cochlear's mission is to help people hear and be heard. Around the world, more people chose a Cochlear-branded hearing implant system than any other. A Cochlear Implant is an electronic device that is surgically implanted under the skin near the ear that restores hearing to those who suffer from severe hearing loss. It's an incredible piece of engineering and the only product in the world that restores a sense through technology. Imagine using your experience to help people around the world to hear again. We can offer a unique opportunity to join Cochlear, an iconic Australian company, leading the world in implantable hearing solutions. Our mission is to help more people to hear. 科利耳是全球领先的植入式听力解决方案专家。我们的使命是帮助人们聆听声音同时帮助他们被聆听。在全球选择科利耳听力植入系统的人是最多的。人工耳蜗是一种电子设备，通过手术将该设备植入耳朵附近的皮肤下，以帮助患有严重听力损失人群恢复听力。这是世界上唯一能够运用技术恢复感官的产品，是一项令人难以置信的工程。想象一下，你能够运用自己的经验去帮助世界各地的人们重获听力。我们可以提供这一独特的机会，加入科利耳，一家标志性的澳大利亚公司，在可植入听力解决方案方面引领世界。我们的使命是帮助更多的人获得听力。 Cochlear Medical Device (Chengdu) Co., Limited is a wholly-owned subsidiary of Cochlear Co., Ltd. in China. It was established in Tianfu New Area, Chengdu, Sichuan Province in September 2017. As Cochlear's only manufacturing site in China, it mainly produces cochlear implants and sound processors, providing professional assistance to the hearing impaired in China and other markets 澳科利耳医疗器械（成都）有限公司是科利耳有限公司在中国成立的全资子公司，于2017年9月在四川省成都市天府新区成立。做为Cochlear在中国唯一的制造中心，主要生产人工耳蜗植入设备和声音处理器，为中国及其他市场的听力损失人士提供专业帮助。 In order to help Cochlear bring products to market that help people with hearing loss, we are recruiting to support the new manufacturing site in Chengdu China. 为了将产品推向市场来帮助有听力损失的人群，我们正在为成都工厂招聘一名。 This role will be based in Chengdu, China. In this role you'll have the opportunity to make a significant contribution to Cochlear's successful history by applying your knowledge and experiences. 该岗位工作地点为中国成都。在该岗位上，您将有机会运用自己的知识和经验为科利耳的成功做出重大贡献。 . Position Overview / Purpose 职位概述 The role of Manufacturing Support Engineer is to provide engineering support to manufacturing in order that manufacturing targets are met and to implement improvements in the Manufacturing areas. 制造支持工程师的职责是为制造团队提供工程支持，以实现生产目标，并在生产区域内落实改进方案。 Accountabilities 主要职责 Accountability 1: Manufacturing support 职责 1 ： 制造 支持 Analyze manufacturing rejects as required to reclaim where possible, identify, and rectify root causes of rejects. 根据需要对生产中的不合格品进行分析，在可能的情况下进行回收，找出导致产生不合格品的根本原因并加以纠正。 Provide fast response or solutions to day-to-day specific manufacturing problems raised in the Fast Response meetings. 针对快速响应会议上提出的日常生产具体问题，提供快速响应解决方案。 Provide equipment and product process related training to team member and ensure the effectiveness of the training. 为团队成员提供设备和产品工艺相关的培训，并确保培训的有效性。 Responsible for supporting Manufacturing to increase manufacturing capacity and yield. 负责支持制造部产能和良率提升。 Responsible for Validation & Verification planning, execution and reporting. 负责验证和确认计划的执行和报告。 Ensure NCRs, Concessions and Change Notice are processed in a timely manner. 确保NCR、让步和变更记录得到及时处理。 Take responsibility of translations and reviewing Work Instructions/Procedures when QMS and DMRs upgrades are required. 根据需要，在 QMS 和 DMR升级时负责翻译及审核工作。 Backup other Manufacturing Support Engineers when resources are constrained or skill overlap is required. 当考虑到存在资源受限或技能重叠的情况时，增援其他制造支持团队。 Accountability 2: Project Work 职责 2 ：项目工作 Execute projects to maximise manufacturing efficiencies on existing manufacturing processes, including the selection of appropriate equipment. 执行项目以最大限度地提高现有生产流程的生产效率，包括选择适用的设备。 Take responsibility of NPI projects, eg. New product, new process, new equipment. 负责 NPI 项目实施，例如新产品、新工艺、新设备。 Execute projects to review and improve manufacturing "indirect" processes. Such as paperwork, bar-coding etc. 执行项目以评审和改进生产"间接"流程，如文书工作、条形码相关工作等。 Accountability 3: Point of contact for other departments 职责 3 ：作为面向其它部门的对接人 Monitor progress of improvement plans and provide feedback to interested parties. 监测改进计划的实施进度，并向相关方提供反馈。 Accountability 4: Compliance to regulations 职责 4 ： 合规性 Ensure that Good Manufacturing Practice (GMP) is followed. 确保遵循质量管理规范 (GMP) 开展工作。 Ensure all documentation meets the requirements of the QMS. 确保所有文件都符合质量管理体系的要求。 Responsible for rectifying issues identified in the audited areas under one's responsibility, and supporting other areas as required.负责审核后的所负责区域问题发现项整改，并根据需要支持其他区域。 Team Role (Individual contributor) 团队角色（个人贡献者） : Follow relevant quality procedures in order to deliver high quality products and services . I dentify and support the implementation of continuous improvement. Undertake additional quality responsibilities (e.g. audit) when appropriately trained and being competent. 遵循相关质量规程，交付优质产品和服务。 识别改进机会，支持开展持续改进工作。在接受了相应工作培训，足以胜任的情况下，担负额外的质量职责（例如审核）。 Contribute ideas on systems and process methods to improve deliverables. 针对系统和流程方法献计献策，以提高可交付成果的质量。 Work safely, complying with all safety procedures, rules and instructions; and reporting workplace hazards,

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