• Maintain and improve Integrated Management System in compliance with Medical Device law and Corporate QMS
• Manage GMP regulation/requirement and maintain the certification to ensure the compliance
• Maiintain post-market surveill;ance activities
• Maintain Medical Device Tracking management system
• Reporting of Medical Device importing, repairing, distributing records and QMS status to relevant organization
경력 및 자격요건
- 5 ~ 8 years experience at QA medical device
- Knowledge of Korean medical device affairs act and MFDS regulation Preferred Qualifications (Certificates, preferred school major, years of work experience, etc.)
- Training for ISO, Quality manager, KGSP etc.
- Good documentation and strong communication skill in Korean and English
- Eager to learn something to be developed
- Willingness to cooperate with other department of the company
기타
- 원서 마감후 1차(서류) 합격자에 한하여 개별연락
- 이력서에 연락처, 희망연봉 게재
- 해외여행에 결격 사유가 없는 자