宜昌招聘

职位描述：
- To make regulatory documents with high quality and manage regulatory processes to ensure competitive approvals of assigned new products and marketed products.


- To close communicate with external regulatory stakeholder to ensure appropriate input and gain rapid approval of submissions.


- To provide proactive regulatory advice and expertise to the cross functions and within RA team.


- To ensure crisis management program implemented and functioning.


- To identify and present option for risk mitigation to decision makers.


- to monitor external evnironment, to proactively identify issues or problems, and to drive change on projects issues.








7-10 years experience in Regulatory Affairs within pharmaceutical industry, global companies experience and or development experience is preferable.


ability to lead cross functional collaboration.


Excellent verbal and written communication and presentation skills with the ability to speak and write clearly and convincingly in English and or Japanese


Master degree in a scientific discipline such as pharmacoanalysis, pharmaceuticals, medical, biology.







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    第一三共集团是一家具有百余年历史的跨国制药企业，总部位于日本东京，全球约有1.5万名员工。在全球范围内专业从事各类医药产品的研究、开发、生产和经营的多元化制药集团。

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