研发工程师
纽迪希亚制药（无锡）有限公司
- 公司性质：外资(欧美)
- 公司行业：制药/生物工程
职位信息
- 发布日期：2017-02-18
- 工作地点：无锡-无锡新区
- 招聘人数：1人
- 学历要求：本科
- 语言要求：英语 良好
- 职位类别：医疗器械研发
职位描述
职位描述：
Excellent understanding of the relevant international and national (ISO, EN) standards related to the design and development of components, sub-assemblies and finished products for medical enteral applications. Principles of Usability Engineering standard and design for manufacturing should be understood and applied.
准确深入了解医疗行业零件和成品的相关设计的国内国际ISO标准，熟悉并掌握与标准相关的产品测试要求。
Based on the ISO standards or input and requirements from local and global marketing, manufacturing, legal, quality and sourcing department, generate ideas as to improve the design of existing products or design ideas for the new products.
能够根据标准要求，以及市场，法律法规，生产，质量及采购等相关部门的输入，完成现有零件，部件及成品的相关优化设计和新产品的设计。
Accurate 2D and 3D output for the related project, ensure the design fully comply the function ,legal, regulatory and project needs, and provide the valuable design for innovation.
对相关项目的产品进行2D和3D的设计输出，确保设计的产品符合性能，法律法规以及项目要求，并能提供有价值的有创造性的设计改进和创新。
Good communication with global team. Work closely together with Europe and China RD teams as well as the operational and engineering teams within Wuxi as to secure design transfer is validated when transferred into production.
配合欧洲设计团队完成所有产品设计从欧洲到中国的转移，并和欧洲团队有着良好的沟通。
Drafting or giving input to the U&DR, Design Input / Output, validation & verification and getting the approval from Europe R&D center and other central functions as documented in the QMS. Following the applicable procedures.
起草或参与设计的输入, 输出, 验证文件得到欧洲R&D总部及其他相关职能部门的批准，并跟进后续的执行。
Support the creation, approval, release, filing and updating of the product specification and production master file (PMF). Support the database and drawing maintenance as to assure the latest versions of these documents are used.
支持产品的标准和产品主文件的制作，审批，发行，归档，升级。 负责数据库和图纸的维护，保证所有文件都是最终的版本。
Provide the strong support for the specification (OASIS) system, PMF and artwork design, update and maintenance.
对产品文件系统OASIS和产品包装的Artwork的设计，管理和维护做相关支持。
Other duties disposed by N+1 supervisor or manager.
上级主管或经理安排的其它工作。
举报
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Excellent understanding of the relevant international and national (ISO, EN) standards related to the design and development of components, sub-assemblies and finished products for medical enteral applications. Principles of Usability Engineering standard and design for manufacturing should be understood and applied.
准确深入了解医疗行业零件和成品的相关设计的国内国际ISO标准，熟悉并掌握与标准相关的产品测试要求。
Based on the ISO standards or input and requirements from local and global marketing, manufacturing, legal, quality and sourcing department, generate ideas as to improve the design of existing products or design ideas for the new products.
能够根据标准要求，以及市场，法律法规，生产，质量及采购等相关部门的输入，完成现有零件，部件及成品的相关优化设计和新产品的设计。
Accurate 2D and 3D output for the related project, ensure the design fully comply the function ,legal, regulatory and project needs, and provide the valuable design for innovation.
对相关项目的产品进行2D和3D的设计输出，确保设计的产品符合性能，法律法规以及项目要求，并能提供有价值的有创造性的设计改进和创新。
Good communication with global team. Work closely together with Europe and China RD teams as well as the operational and engineering teams within Wuxi as to secure design transfer is validated when transferred into production.
配合欧洲设计团队完成所有产品设计从欧洲到中国的转移，并和欧洲团队有着良好的沟通。
Drafting or giving input to the U&DR, Design Input / Output, validation & verification and getting the approval from Europe R&D center and other central functions as documented in the QMS. Following the applicable procedures.
起草或参与设计的输入, 输出, 验证文件得到欧洲R&D总部及其他相关职能部门的批准，并跟进后续的执行。
Support the creation, approval, release, filing and updating of the product specification and production master file (PMF). Support the database and drawing maintenance as to assure the latest versions of these documents are used.
支持产品的标准和产品主文件的制作，审批，发行，归档，升级。 负责数据库和图纸的维护，保证所有文件都是最终的版本。
Provide the strong support for the specification (OASIS) system, PMF and artwork design, update and maintenance.
对产品文件系统OASIS和产品包装的Artwork的设计，管理和维护做相关支持。
Other duties disposed by N+1 supervisor or manager.
上级主管或经理安排的其它工作。
职能类别： 医疗器械研发
公司介绍
纽迪希亚于1995年进入中国市场，并于2000年1月设立工厂并正式投产。这是一家向欧美市场出口肠内营养产品及配套产品的公司，同时也是纽迪希亚全球三大生产基地之一。
纽迪希亚是中国肠内营养理念推广与传播的先行者，目前已经完成了 研发、生产、营销、服务等完整产业生态链的建设。公司主要生产经营肠内临床营养产品（ECN）,肠内营养输注产品（Flocare）以及特殊医学用途配方食品（FSMP）。
纽迪希亚坚持以患者为中心，携手政府、医疗机构等社会各方力量，致力于通过创新的产品和业务模式，推动中国医学营养产业的发展，帮助患者延长生命，享受更健康，更有尊严的生活。
纽迪希亚是中国肠内营养理念推广与传播的先行者，目前已经完成了 研发、生产、营销、服务等完整产业生态链的建设。公司主要生产经营肠内临床营养产品（ECN）,肠内营养输注产品（Flocare）以及特殊医学用途配方食品（FSMP）。
纽迪希亚坚持以患者为中心，携手政府、医疗机构等社会各方力量，致力于通过创新的产品和业务模式，推动中国医学营养产业的发展，帮助患者延长生命，享受更健康，更有尊严的生活。
联系方式
- Email：HRA@nutricia.com