职位详情

注册经理 RA manager

面议

北京 3-5年 本科
西安杨森制药有限公司

医药企业 其他 规模不详

职位描述
Responsibilities:
1. Cooperates with headquarter an******** to establishes registrationplan an********.
2. Provides guidance an******** to subordinates on regulatory affairs toensure registration projects complete********.
3. Interact with HA off******** reviewers an******** an******** training
4. Actively involve******** establishment an******** of regulat********guidelines an******** drug standards.
5. Develops internal policies an********.
6. Support function departments on new product launch an********. 
7. Handles crises relate******** regulatory affairs.
8.  Actively involve******** Cross functional activities

Qualification********
A university degree major in chem******** pharmaceut******** biology ora relate********-science discipline. A master degree or above ispreferable.
2. At least 5 years of regulatory affair experience including 2 year inmanagerial role in a multinational pharmaceutical company.
3. Strong lobby capability an******** communication skill; excellentleadership with team spirit; high learning ability an******** to workunder stress an******** challenges.
4. Have goo******** with HA.
5. Fluent English in verbal an********; goo******** skill.
职位要求
  • 专业要求: 临床医学
  • 最低学历: 本科
  • 工作年限: 3-5年
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