1. Manage regulatory affairs projects under his/her responsibilities agreed with RA manager and Head of Division
2. Ensure product life cycle management and post approval change controls are done as required for the project s under his/her responsobility
3. Establish and maintain collaborative relationship with CoE GRA and internal stakeholders, as well as external stakeholders
4. Manage RA budget for responsible regulatory projects
5. Provide regular monitoring and business impact analysis of regulartory environment changes and share them with wider group as required to ensure alignment

-4years university degree in life science or medical engineering
-Minimum 5years relevant experience in medical device industry
-Multinational company experience preferred
-Experience of leading project preferred

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