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【实习】Regulatory Affairs Intern医药注册实习生
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楼主 发表于  2016/4/11 13:35:01    编 辑   

关于GE 
GE,想到,做到。
GE专注于世界至关重要的需求,以卓越人才和领先技术,致力解决最具挑战的议题,提供包括能源、医疗、照明、航空、交通运输和金融等广泛领域的解决方案,我们构建、驱动、载运、医治,创想为本,行重于言。
只为一个共同的愿景:一个更美好的世界。GE开创了连通现实生活和数字世界的新渠道。在我们的研发中心、我们的制造工厂、我们的客户面前,GE时刻致力于引领全新的工业时代 —— 一个能让这个世界更有活力、更有创造力、更健康的时代。

Intern Job Responsibilities 实习生工作职责:
1. Responsible for all department admin (pay fees, stationery application, book meeting, etc.)
2. Support China RA activities such as submit documents, receive licenses, etc. and part of documents translation.
3. Assist to prepare and submit CPP/CFS documents to authorities or the notary office/ the consulate.
4. Assist all SOP related activities (archive, periodic review & revision for RA SOP, change RA SOP into WPs etc.)
5. Responsible for scan and archive all RA Documents (license distribution, the database maintenance of product registration and material and trademark, documents archive etc.)
6. Assist RA team on registration documents preparation, translation and checking according to Chinese regulation.
7. Finish other assigned tasks by department.

Intern Hiring Quality 实习生招聘要求:
1. Outstanding undergraduate or postgraduate students or
2. Fluent English reading and speaking
3. Proactive, can-do attitude, responsible, good learning attitude on Industry environment
4. Familiar with office software operation
5. Good communication and coordination skill

Office Location in Chinese 工作地点:中国上海浦东张江高科技园区华佗路1号
补贴:本科 110/day  研究生130/day

如果,你想积累实习经验,五百强顶级公司等你来投!如果你想开拓眼界,为以后职业规划打好基础,在这里你可以接触最顶级的职场人士,最优秀的工程师,以及最nice的员工
若感兴趣 简历请以“姓名- 医药注册实习生-每周实习天数-可以实习月数-最快上岗时间”标题形式投yuelei.jin@ge.com
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