泰科医疗器材制造（上海）有限公司

职位描述：
·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