• Plan and execute reimbursement strategy
• Lead new product registration with KFDA for imported medical device and drug/quasi-drug
• Support quality management system in compliance with regulatory requirements



Responsibilities include:

• Lead projects with strategic thinking of reimbursement service
• Understand related laws & regulations and facilitate regulatory compliance
• Support regulatory documentation for outsourcing products registration in Korea and our commany subsidiaries
• Revise and update the product registration due to the changes requiring regulatory actions

• Prepare for the audits by government and participate in the internal audit of quality management system

- Experience of reimbursement strategy for medical device, quasi-drug and drug
- Good communication skill with related authorities
- English communication skill(written and spoken)
- 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