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    Regulatory Affairs Specialist - Irvine, United States - Cypress HCM

    Cypress HCM background
    Upper Management / Consulting
    Description

    · 0-2 years of experience in regulatory affairs, and/or experience in QA, R&D, Manufacturing or Project Management within the IVD industry

    · Working knowledge of FDA, and CE marking requirements for IVD products is a plus

    · Able to work independently and with others

    · Able to work with minimal supervision

    · Excellent computer applications skills

    · Strong customer orientation and focus

    Salary: 90K



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