담당업무
ㆍEnsure a Quality system is in place in compliance with Regulatory and ISO standards.
ㆍLead QA organization * Expertise in ISO, GMP international standards. * Make release decisions of finished products.
자격요건
ㆍ학력 : 대졸이상/Biological, Immunization등 진단메카니즘을 이해할 수 있는 전공.
ㆍ경력 : 경력15년↑/Pharmaceutical, Medical Device, IVD * Experience in IVD with understanding of ISO 13485-2016, EU 2017/746(IVDR) and other rapid diagnostic device related international requirement. * Good command of English
* 필요서류 : 영문resume * 보내실 곳 : e.mail / jiko01@kohuman.com * 담당자 : 고 재익 010 8636 5759
우대사항
ㆍ
ㆍ
|