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

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