JOB RESPONSIBILITIES

工作职责

• Owner of product documents, responsible to maintain and update product related documents (DMR, drawing,/specifications, engineering change control etc).

  产品文件负责人，负责和维护以及更新产品相关的文档。

• Support raw material localization, join in qualification activities .

  支持原材料本地化以及验证。

• Supporting production, failure analysis of products that from line and field. Work out corrective actions and preventive actions.

  支持生产以及进行产品失效分析和纠正预防措施。

• Validation activities, IQ, OQ and PQ

分别支持安装确认、运行确认、性能确认

• Improve manufacturing process

  改进生产制造工艺

• Appraises technological developments and investigates feasibility of new equipment and techniques.

  评估技术发展以及新设备和技术可行性评估。

• Set up BOM and item master, maintain product BOM and item master in Agile product lifecycle management system

  建立原材料清单并在Agile系统内进行维护

WORK ENVIRONMENT

工作环境

Domestic and oversea traveling request. 国内/外出差要求

JOB QUALIFICATIONS

岗位资质

• Knowledge / Education 教育背景

Engineering and Electronic/mechanical technology education background is preferred.

工程及电子机械技术教育背景优先

• Job Experience 工作经验

Minimum 1+ years engineering experience,

Familiar with engineering/ project in Pharmaceutical or Medical Device or related manufacturing.

在医药或医疗器械相关制造并熟悉工程及项目

• Skills / Competencies 技术能力

Quick learning快速学习

• Language / Computer 语言/ 计算机能力

Good written and verbal communication skills in both Mandarin Chinese & English.

中英文听说读写沟通良好

Excellent office skill

办公自动化技能优秀

• Others 其他

GD&T, Auto CAD, Pro-E, SoliderWroks is preferred

上班地址：漕河泾出口加工区