• 1年经验
  • 本科
  • 招1人
  • 11-09 发布
  • 专业培训

职位描述

职位描述: Job Responsibilities:1.Beijing office administrations2.Support to China Regulatory Affairs function, such as:1)Assist RA to print, PDF convert and archive submission dossier, including paper and electronic archive;2)Provide submission dossier and approval docs for HQ RA for record use;3)Artworks internal implementation/transition after CFDA approval;4)Docs. collection, correction, summary, and delivery to others Dept. as requested;5)Compliance role for some simple case, if applicable. Rules in China for promotional is not very complex;6)Routine work, i.e. simple Docs. translation and check, artork comparison, payment request, and others requested by RA.Job Requirements:-Work Period: November 2017 - January 2018-Graduate from Pharmaceutical or Medical Device University preferred, OR academic background of bio or chemistry-related;-Relevant experience in Regulatory Affairs preferred. 职能类别: 药品注册 医疗器械注册 关键字: RA

联系方式

北京

公司信息

自1926年起,加柏集团,这一医疗成像对比剂产品的研究开发领域的先驱者已经建立起了其悠久的传统。加柏公司总部位于法国巴黎,是一家上市公司,其在欧洲对比剂市场的市场份额为25%在全世界的市场份额为7%。加柏充分利用其专业知识及创新能力,迎接21世纪公共卫生领域的重大挑战。我们的团队为重大疾病(癌症,心血管、感染,神经变性疾病)的诊断技术进步做出了卓越的贡献。我们新型高效的成像解决方案为全世界的患者保证了更好的治疗方案。

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