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Responsibilities:
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.
Required Qualifications:
1. Outstanding undergraduate or postgraduate students
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. Major in medicine and pharmacology
工作时间:一周3天以上,六个月
工作地点:上还是浦东新区张江高科技园区华佗路1号
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- (SH)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ziwei.liao@ge.com |
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