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泰科医疗器材制造(上海)有限公司

(全职,发布于2007-05-16) 相关搜索
  • 工作地点:上海
  • 职位:法规事务专员 Regulatory Affairs Specialist
  • 信息来源:中华英才网
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·Track all new and existing product development for broad range of product categories.
·Conduct meetings with Engineering and Marketing personnel to assess/assign critical elements for new product submissions to SFDA and international authorities.
·Communicate with THC regional and division regulatory regarding submission approval status/issues for pending submissions.
·Coordinate and compile product registration dossiers
·Develop regulatory strategies and SOP
·Provide assistance during SFDA and other regulatory agency inspections. Develop regulatory strategy for responding to SFDA and other regulatory agency’s observations.
·Generate/revise, proofread and review labelling (container labels, package inserts, carton labelling)
·Responsible for routing of product complaints, including investigation and written response to complainant upon completion


A bold attempt is half success. 勇敢的尝试是成功的一半。 ,www.yingjiesheng.com