Regulatory Affairs Specialist - Cotia - beBeeRegulatory

    beBeeRegulatory
    beBeeRegulatory Cotia

    há 3 semanas

    Título do emprego: Regulatory Affairs Specialist

    Descrição

    Join Amaris Consulting's dynamic team as a Regulatory Affairs Specialist. This role involves leading activities related to medical devices, ensuring compliance with European regulations.

    Your Missions:

    • Lead regulatory affairs activities for medical devices ensuring EU MDR compliance.
    • Demonstrate expertise in medical device classification (Class IIa & IIb), applying relevant rules accurately.
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