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EMEA Regulatory Affairs Specialist– Medical Devices, Dublin

EMEA Regulatory Affairs Specialist– Medical Devices, Dublin
Description
Teleflex is seeking a qualified individual to support regulatory activities for medical products in the EMEA region. The role involves ensuring compliance with regulatory standards, coordinating product registrations, and preparing submission files. Candidates should have a degree in Science or Engineering, along with at least 3 years of experience in the medical device industry.Effective communication and organizational skills are required, with a focus on regulatory compliance and collaboration with various stakeholders.

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Highlights
  • Company name
    Teleflex
  • Job position
    EMEA Regulatory Affairs Specialist– Medical Devices
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