• 5-7年经验
  • 本科
  • 招1人
  • 01-23 发布

职位描述

Essential Responsibilities Key responsibilities include: •Drive improved product quality by identifying manufacturing issues, developing cost-effective solutions, and overseeing successful implementation into production. •Work with Production Associates to resolve manufacturing and quality problems related to methods, processes, tooling, equipment and product design. •Troubleshoot production issue and provide Technical support •Ensuring regulatory compliance through Validation & Verification. Responsible for determining processes requiring validation, development of plans and analysis criteria, execution and final analysis and acceptance. •Develop new process and layout designs to reduce cycle time and support the lean manufacturing initiative. •Monitor and improve productivity, while ensuring all customer commitments are met in a timely, quality and cost-conscious manner. •Co-ordination of manufacturing releases per engineer change request. •Lead Compliance, as well as Environmental, Health & Safety efforts in support of plant goals •Driving LEAN manufacturing implementation About Us GE is the world's Digital Industrial Company, transforming industry with software-defined machines and solutions that are connected, responsive and predictive. Through our people, leadership development, services, technology and scale, GE delivers better outcomes for global customers by speaking the language of industry. Role Summary/Purpose Provide technical support for the production team. Responsibilities include providing documentation and floor support associated with safety, manufacturing and quality methods, tooling, and equipment. Aggressively initiate new processes and methods that will improve safety, productivity, reduce product cost and/or improve product quality. Qualifications/Requirements Quality Specific Goals: 1.Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position 2.Complete all planned Quality & Compliance training within the defined deadlines 3.Identify and report any quality or compliance concerns and take immediate corrective action as required 4.Knowledge and understanding of document control, design transfer, verification, validation, acceptance activity, DMR, DHR and electronic signature requirements to ensure that product, equipment, tools, processes, software, training and documentation meet requirements. Qualifications: •B.S. Degree in Mechanical, Electrical, Industrial Engineering or related technical degree with 5 years of experience in supply chain or engineering. •Demonstrated experience owning production processes, and growing capability, yield and quality. •Good data analysis skill or Six Sigma skills in DMAIC •Good communication Skills with different function team including engineer, supply chain. Desired Characteristics Preferred Qualifications: 1. M.S. Degree in Engineering or Business 2. Demonstrated ability to identify & implement best practices. 3. Demonstrated ability to perform with high levels of ambiguity 4. 6-sigma DMAIC GB/BB certified 5. Demonstrated program or project management skills 职能类别: 其他

联系方式

公司信息

GE医疗集团通过提供革新性的医疗技术和服务,开创医疗护理的新时代。GE医疗在医学成像、信息技术、医疗诊断、患者监护系统、药物研发、生物制药技术、卓越运营和整体运营解决方案等领域拥有广泛的专业技术,能够帮助客户以更低的成本为全世界更多的人提供更优质的服务。 GE医疗从1979 年开始在中国开展业务,于1986年在北京成立了第一个办事处。GE 医疗在中国建立了包括独资和合资企业在内的多个经营实体,拥有员工 4,500 多名。GE 医疗在中国共拥有七个全球生产基地:在北京建有CT扫描系统、磁共振成像系统 和 X 光成像系统工厂,在上海有生命科学基地,在无锡建有超声和患者监护仪设备工厂,在桐庐建有滤纸生产基地,在深圳建有医用面罩生产基地。其中,在北京的GE(中国)医疗工业园区,占地 6万平方米,是 GE 医疗集团全球最大的生产和研发基地之一。

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