高级法规事务专员-Sr. RA Specialist-北京
美国泰利福医疗Teleflex Medical 查看所有职位BeijingUpdate time: May 27,2019
Job Description

PART I - PRINCIPAL RESPONSIBILITIES 主要职责

  • Chinese IFU/label drafting
  • RA document management
  • Master database maintain (Kindie system, SLC database, SLC database)
  • Set RA SOP to ensure regulatory compliance
  • Internal NEO trainer
  • Provide regulatory support to related function (QA, DP, Supply chain and local BU)


PART II – QUALIFICATIONS 任职要求

1, Bachelor degree and above

2. RA working experience is preferred

3. excellent communication skill in Chinese and English


4. have strategic thinking and project management


OTHER QUALIFICATIONS (Physical, Visual etc.) 其他要求

1. common communication in Chinese and English

2. Carefulness, preciseness, initiative and strong rationality, strong sense of responsibility and team work

职能类别: 医疗器械注册 政府事务管理

关键字: 医疗器械 美资 外企 产品注册 法规事务

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上班地址:朝阳区酒仙桥路20号颐堤港一座2层208室

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