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    Quality & Regulatory Associate - Leeds, United Kingdom - Kenton Black - Science & Engineering

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    Description

    A fantastic opportunity is available for a Regulatory Affairs Associate to join a thriving and expanding medical device company based in West Yorkshire.

    The main responsibility of this role swill be to ensure that the regulatory requirements of the company are met in line with project deadlines.

    Determine regulatory pathways for product registration in various global countries

    • Perform medical device regulatory compliance gap analyses and implementation.
    • Provide Regulatory input on project teams for projects including but not limited to new product development, continuous improvement, regulatory compliance.
    The ideal candidate for this role will have a proven track record within the Medical Device sector.
    Knowledge/understanding of EU Medical Device Regulations (MDR) and MDSAP regulations
    BSc (or equivalent) in a Life Science or related field.


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