-Prepare submissions for the new product registration
-Initiate, track and facilitate new product registrations and achieve on-time approvals
-Ensure maintenance of registered product license
-Maintain a close working relationship with Government authorities for the product registration
-Monitor regulatory environment changes, and provide impact analysis plus action plans to ensure compliance
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-Minimum 3 years in regulatory affairs of medical devices
-Preferred majors in priority : medical science, biology, engineering etc.
-Effective communication skill
-Comprehensive knowledge of regulation
-Good computer skill
-Fluent written and spoken English

- 원서 마감후 1차(서류) 합격자에 한하여 개별연락
- 이력서에 연락처, 희망연봉 게재
- 해외여행에 결격 사유가 없는 자