• 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
경력 및 자격요건
- 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
기타
- 원서 마감후 1차(서류) 합격자에 한하여 개별연락
- 이력서에 연락처, 희망연봉 게재
- 해외여행에 결격 사유가 없는 자
담당업무
입사지원
돌아가기
02-6281-5034
jsb@nterway.com
