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¤ý Prepare and file appropriate regulatory submissions for new product registration¤ý Review product and process changes, and product documentation to assure regulatory requirements compliance, consistency, and accuracy¤ý Maintain up-to-date knowledge of regulatory requirements¤ý Interacts with MFDS and/or other regulatory bodies for submissions and projects
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ü 3-7 years¡¯ experience in Regulatory Affair related Medical deviceü Experience with ME equipmentü Experience in QA and/or Reimbursementü Proficiency in speaking, reading and writing Englishü Full knowledge and understanding of regulations relevant to medical devices
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