泰州招聘

职位描述：
职位描述：
一、 岗位描述
Develop new technology, products, materials, processes, or equipment with minimal supervision. Independently, or as a member of a team, develops, directs, and utes 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 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 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。

Assess 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

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

Project Management: Workcooperatively with process development, quality, manufacturing, regulatory, clinical, and marketing on complex projects to ensure project success. Be skilled with Project.
X项目管理：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, 熟练运用project.
Process validation & new productverification and validation, product FMEA, risk management.
产品过程验证和研发验证,风险分析和控制。

Process capability analysis； be skilled in Minitab to do data statistics
制程能力分析,熟练应用Minitab做数据分析。

Be familiar with ISO13485 and medical device quality system.
熟悉ISO13485，医疗器械质量体系。

三、Qualifications:
资质：
BS in Engineering (mechanical or related)
工程学士学位
At least 3 years Medical device experience
三年以上医疗行业经验者优先
English required
英语熟练 举报 分享

赛昂国际医疗技术(中国)有限公司Scion Medical Technologies (China) Ltd.是由SCION MEDICAL LIMITED（赛昂国际医疗控股有限公司）于2011年10月在中国大陆投资创办的外商独资企业，中国运营总部和工厂位于中国医药城。赛昂中国一期投资壹亿人民币，生产面积7000平米，计划建设4条生产线和1个研发中心。
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。