- Perform product registration (mainly medical devices) and regulatory affairs according to the relevant regulations
- Prepare and maintain artworks of Korean product labels and leaflets
- Maintain up-to-date registration documents and registration database
- Monitor new technologies and any regulatory changes which may have potential regulatory/business impact
- Achieve the best results by effective communication and negotiation with internal/external stakeholders
지원자격
- 약학/화학/생물계열 전공자 (약사면허소지자 선호)
- 의약품 또는 의료기기 RA 업무 2년 이상 경력자
- Fluent in English