1. Lead new product registration with KFDA for imported medical device and drug/quasi-drug
2. Support quality management system in compliance with regulatory requirements
3. Understand related laws & regulations and facilitate regulatory compliance
4. Support regulatory documentation for outsourcing products registration in Korea
5. Revise and update the product registration due to the changes requiring regulatory actions
6. Prepare for the audits by government and participate in the internal audit of quality management system

1. Pharmacist's license or major in related field and have medical background
2. Good communication skill with related authorities
3. English communication skill(written and spoken)
4. Knowledge of RA including product registration, QA procedure or reimbursement price system

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