无锡相关职位: 研发工程师(高通量测序方向) 研发工程师(分子生物学方向) 临床研究项目主管 临床研究项目经理 医学主管 销售代表+包住宿+带薪培训 医疗器械销售推广(多城市) 医疗器械销售推广(多城市) 跟单员及内勤 QA/QC/暖通调试工程师
周边城市招聘: 上海 浙江 安徽 广东 山东 河北 重庆 北京 江苏 湖南
企业入驻日期: 2017-11-09
Essential Responsibilities Key responsibilities/essential functions include: • Drive improved product quality by identifying manufacturing issues, developing advanced manufacturing cost-effective solutions, and overseeing successful implementation into production • Work with manufacturing leadership to identify and resolve manufacturing and quality problems related to methods, processes, tooling, equipment and product design • Monitor and improve productivity throughout the use of Lean Six Sigma or related tools, while ensuring all customer commitments are met in a timely, quality and cost-conscious manner • Participate in early focus on manufacturability in NPI and/or Advanced Technology programs. Drive rigor in process capability assessment, process layout, tooling and equipment development • Clearly understand existing processes in order to provide support for manufacturing process technology roadmap • Ensure regulatory compliance through Qualification & Validation. Responsible for ensuring rigor in determining processes requiring validation, development of plans and analysis criteria, execution and final analysis and acceptance 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 To accelerate progress of our Brilliant Factory deployment we are building a BF focus team that will support the site’s strategy. They will partner with Operation and COE leaders to accelerate progress, leverage best practices across site, driving process and performance rigor. Strengthen the technical capabilities for the production teams. Aggressively initiate new processes and methods that will improve safety, reduce product cost and 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 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 1. Bachelor's Degree in Computer Science, Electrical Engineering or Automation Control related Subject 2.Experience in PLC oriented design methodology 3.Experience in programming with C/C++, COM, STL, ATL, Multi-Threads 4.Experience in programming with Windows System 5.3+ year experience in software development 6.Demonstrated troubleshooting, analytical and planning skills 7. Ability to work independently 8. Demonstrated strong communication skills (written and verbal) Desired Characteristics 1. MS/PHD in technical concentration/field 2. Electronical backgrounding with at least 3 years on industry automation design/delivery; 3. Experienced on PLC/sensor enable/labVIEW; 4. 6-sigma DMAIC & DFSS certified 5. Experiences in Process Intensive manufacturing 6. Product and Process Development experience 7. Experienced developing tools and templates 8. Demonstrated program or project management skills 9. Demonstrated experience owning production processes / growing capability in yield and quality 10. Experience working with global teams Desired Characteristics -Experienced on pneumatic assembly/testing/failure analysis; - Solid working knowledge of GEHC QMS procedures for GMP 职能类别: 其他
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。
学术主管 6-8千/月
益生菌项目经理 7-7千/月
产品经理 1-1.5万/月
产品经理 1-1.5万/月
销售代表 1-1.5万/月
销售代表 1-1.5万/月
销售代表 1-1.5万/月
产品经理 1-1.5万/月
工程部经理(工艺设备维护) 1.5千以下/月
学术推广员-无锡办事处 6-8千/月
渠道经理(分子生物试剂) 6-8千/月
渠道经理(分子生物试剂) 6-8千/月
渠道经理(分子生物试剂) 6-8千/月
QC实验室设备管理员 6-8千/月
Pi Software Engineer 0.6-1万/月
无锡相关职位: 研发工程师(高通量测序方向) 研发工程师(分子生物学方向) 临床研究项目主管 临床研究项目经理 医学主管 销售代表+包住宿+带薪培训 医疗器械销售推广(多城市) 医疗器械销售推广(多城市) 跟单员及内勤 QA/QC/暖通调试工程师
周边城市招聘: 上海 浙江 安徽 广东 山东 河北 重庆 北京 江苏 湖南
企业入驻日期: 2017-11-09