高级工程师
赛昂国际医疗技术(中国)有限公司
- 公司规模:50-150人
- 公司性质:外资(欧美)
- 公司行业:医疗设备/器械
职位信息
- 发布日期:2017-05-22
- 工作地点:泰州
- 招聘人数:1
- 工作经验:五年以上
- 学历要求:本科
- 语言要求:英语
- 职位月薪:面议
- 职位类别:医疗器械研发 医疗器械生产/质量管理
职位描述
一、 岗位描述
Develops new technology, products, materials, processes, or equipment with minimal supervision. Independently, or as a member of a team, develops, directs, and executes plans for a major segment of complex projects. Compiles and analyzes operational, test, and research data to establish technical specifications for designing or modifying products, processes, and materials.
开发新技术、产品、材料、过程或设备用的基本管理。作为独立或团队的一员能开发,指导,执行项目计划的主要部分。能编辑和分析操作、测试和研究数据建立、设计或修改产品的技术规格,流程和材料。
二、Key Responsibilities
主要职责
Consistently generates innovative and unique solutions to market needs and submits idea disclosures. Work is expected to result in the development of new or refined products, processes or equipment.
能不断创造、创新和独特的符合市场需求的解决方案并提交发布。希望能研发新产品的或优化产品、工艺或设备。
Successfully completes complex engineering work in one or more of the following: technology development, product design and development, test of materials or products, preparation of specifications, process study, research investigation (animal and clinical studies), and report preparation.
能成功完成复杂的技术工作在一个或多个条件下:如:技术开发、产品设计和研发、材料测试或产品测试、各项准备工作、过程研究,调查研究(动物和临床研究),并准备报告。
Selects techniques to solve complex problems and make sound design recommendations.
能选择相应的技术来解决重要的问题和制定合理的设计建议。
Summarizes, analyzes, and draws conclusions from complex test results.
对重要测试的结果进行总结、分析并给与相关结论。
Designs and prepares complex reports to communicate results to technical community.
在技术交流时设计和准备测试报告并分享结果
Designs and coordinates complex engineering tests and experiments.
设计和协调复杂的工程测试或实验
Coordinates, manages, and documents project goals and progress and recommends appropriate revisions.
协调、管理和文档项的目标和进度并建议适当的修正。
Assesses the feasibility and soundness of proposed engineering evaluation tests, products or equipment.
对测试、产品或设备的可行性和可靠性提出工程评估
Interfaces with Physicians/Cath Lab personnel to obtain feedback on concepts and performance of new devices.
就产品的的理念和新设备的性能与医生/疏导实验室人员沟通并获得反馈。
Translates customer needs into product requirements and design specifications.
将客户的需求转换成对产品需求的设计规范
Responsible for engineering documentation.
负责技术文档
Works cooperatively with process development, quality, manufacturing, regulatory, clinical, and marketing on complex projects to ensure project success.
与过程开发、质量、制造、管理、临床、和市场营销在重要项目的相互合作,确保项目的成功。
May train and/or provide work direction to technicians and entry-level engineers.
能对新人(初级工程师)进行培训或提供技术指导
Demonstrates PDP/TPD system knowledge through delivery of high quality and high impact deliverables.
利用PDP/TPD系统相关的知识 贯穿高质量的产品交付
Quality System Requirements
质量体系要求
In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.
在所有行为都是致力于病人安全和产品均服从质量方针和相关的质量记录、品质工程和程序
For those individuals that supervise others, the following statements are applicable:
Assures that appropriate resources (personnel, tools, etc.) are maintained in order to assure Quality
三、Qualifications:
资质:
BS in Engineering
工程学士学位
5+ years direct work experience required
5年管理工作经验
Experience with capital systems and disposable devices is required
要求有资本管理和一次性器械经验
Medical industry experience preferred
有医疗行业经验者优先
SolidWorks experience
SolidWorks 熟练使用
English required
英语熟练
公司介绍
公司利用其在国际医疗器械领域丰富的管理和并购经验和人脉,收购并整合欧美的高端医疗技术并引进中国医药城园区,在园区打造国际化的医疗器械生产基地(园区)。降低生产成本,供应全球市场,在保持欧美销售增长同时,迅速在中国注册和销售并购的高端医疗器材。
联系方式
- 公司地址:上班地址:江苏省泰州市中国医药城,药城三期厂房G32栋