-To ensure proper Resistration of New Products
-Prepare necessary technical documents and other applications
-Periodic renewal of KGMP Certificate including manufacturing site inspection
-KGMP Submission
-GAP Analysis of existing licenses and identifying necessity of any license update
-Regulatory Compliance
-Quality management
경력 및 자격요건
-Bachelor's degree
-More than 4 years of experience with quality and/or regulatory process in medical devices
-IT literacy, experience with using MS office applications
-Strong interpersonal , orgarnizational, and communication skills
-Passion for quality and to do things right
-Language skills: good written and verval English required
기타
- 원서 마감후 1차(서류) 합격자에 한하여 개별연락
- 이력서에 연락처, 희망연봉 게재
- 해외여행에 결격 사유가 없는 자