• To maintain efficient and productive manufacturing support to the production areas through implementation and management of day-to-day production equipment and process improvements.
  通过实施和管理日常生产设备和工艺改进，持续支持生产区的高效生产。
• Leads the Manufacturing Support Team in establishing product technical capabilities and translates product technical requirements into CCD.
• 制造支持团队建立成都工厂产品技术能力以及转化产品技术要求.
• To interact with Manufacturing、Process engineering & Operational Excellence and R&D in the development of new products, product improvements and/or product transfer.
  就新产品开发、产品改进和/或产品转移等方面，与生产制造、工艺工程和卓越运营、研发部门相互沟通.

• You will be overall responsible for the Manufacturing on yield improvement, scrap reduction and process optimization. 全面负责生产制造环节的良率提高，报废降低以及生产工艺的改善。
• Lead complex and technical investigation and be accountable to provide solution to identified production problems.复杂的技术问题的调查，并为已发现的生产问题提供解决方案。
• Make technical decisions in engineering subjects, quality subjects, as well as collaboration across Cochlear organization.有关工程、质量及在科利耳组织内部的合作方面做出技术决策.
• Develop the technology strategy road map for the manufacturing network in order to support the introduction of new product, the transfer of products within the manufacturing network and to maintain Cochlear manufacturing competitiveness.工厂的技术发展战略，以支持新产品的引进和产品的转移，以保持科利耳集团生产竞争力。
• Leading engineers in understanding product and process design principles, to establish manufacturing environment with built in quality during new product transfer.工程师团队理解产品和工艺设计原则，以期建立具有生产合格质量产品的的工艺流程。
• Plan and initiate programs to achieve Operational Excellence in Engineering and Maintenance activities that have impact on productivity, quality, safety, reliability, and cost.以实现对生产力、质量、安全、可靠性和成本的持续改善。
• Insures adherence and compliance to the Quality System and relevant regulatory bodies.质量体系和相关法规.
• Support the Manufacturing/ Process engineering and Manufacturing support group in the creation and maintenance of manufacturing documentation, product configuration, product testing and tooling design and associated documentation throughout the product life cycle.创建和维护应用于产品全生命周期的生产文件、产品配置、产品测试和工具设计以及相关文件。
• Manage day-to-day activities of manufacturing support team to ensure the optimum utilization of resources to maintain reliable and efficient operation.团队的日常活动，确保资源的最佳利用，以保持团队可靠和高效的运行。
• Ensure training metrics are developed and maintained and appropriate development targets are developed for everyone in the team.训计划的制定和维护，并为团队中的每个人制定适当的发展目标。

• Minimum Bachelor’s Degree in Engineering field or equivalent discipline.

• Minimum 5 years of experience in medical device manufacturing environment

• At least 8 years of team management experience, with a team size of no less than 5 people.

• Fluent in English language, both written and oral

• Working exposure to CAPA, NCR, Concession, etc is essential for this role.

• Exposure to product life cycle & product transfer process in a medical device manufacturing environment.

• MUST have demonstrated "hands-on" experience with all facets of production, people, machines and processes.

• Demonstrated experience working on process and systems improvements in a manufacturing through applying lean concepts.

• Demonstrated experience to compliance to WHS practices and regulations.
  在健康/安全/环保方面有丰富的经验。

• Excellent communicate skills, communicate with openness, clarity

掌握出色的沟通技巧，能够开诚布公地与人沟通，表述清晰

• Ability to make quality and timely decisions

• Working experience in precision assembly/ Silicone Injection Molding/ Laser Welding/ Resistance Welding is highly desirable for this role.

• Demonstrated experience in managing external auditors in a manufacturing environment i.e TUV, FDA, TGA, etc.

• Has the ability to build a healthy partnerships with cross-functional partners, business units, and/or sites to achieve common goal.

• Has excellent financial acumen in managing manufacturing operations.