赛默飞世尔科技 · Clinical Research Group临床研究部门

Sr. Regulatory Affairs

薪资面议  /  北京

今天 15:31 更新

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职位属性

  • 招聘类型:社招
  • 工作性质:全职

职位描述

Job Description

Responsibilities:


Be responsible for the registrations of imported drug. Including but not limited to the good communications with NMPA, CDE and other authority, registration documents preparation, performing the test, documents submissions and follow up of NMPA until get the approval. Timely documents archiving. Other tasks if needed.


Minimum Qualifications:


Bachelor degree

At least 2-3 year’s experience on imported drug registration

Good at written and oral English


Preferred Qualifications: Medical education background

The experience on all of API, ANDA, IND and other type registration is preferred

Good communications skill

公司福利

  • 13薪+商业保险
  • 年终奖金
  • 带薪年假
  • 住房、节日津贴
  • 丰富的员工活动