Job Description SummaryJob DescriptionP2-14313Mainly Product License Approval for new and amendment on timePrepares regulatory documents for product submissions. Acquires information from appropriate technical groups and project personnel which addresses performance of medical devices, instrument. Assures adequate documentation exists for product claims and directs timely review of regulatory documents.Demonstrates continuous pursuit of regulatory knowledge to obtain experience and expertise in product submissions and regulatory topicsStrategic communication skill and ability with team, MFDS officer and Business partnerStrategic and meticulous mindset is preferredMinimum 4~7 years prior experience working on product regulatory submissions.Fully understand new and revised Medical device Act
Job Description SummaryJob DescriptionP2-14313
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Required SkillsOptional Skills.Primary Work LocationKOR South Korea - Seoul HQAdditional LocationsWork Shift
