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    Regulatory Affairs Consultant - England, United Kingdom - Michael Page (UK)

    Michael Page (UK)
    Michael Page (UK) England, United Kingdom

    5 days ago

    Default job background
    Description
    Our client is a fast growing medical devices consultancy, specialising in regulatory compliance, patents, clinical investigation and market entry.
    Ensure compliance with all relevant regulatory standards and guidelines within the healthcare industry.
    Develop and implement Regulatory Affairs and Quality Assurance strategies.
    Provide guidance and support to Clients.
    Communicate effectively with regulatory authorities.
    Prepare and submit regulatory documents to appropriate bodies.
    Oversee internal audits and inspections to ensure compliance.
    Collaborate with cross-functional teams to support product development.
    Stay up to date with changes in regulatory legislation and guidelines within the healthcare industry.
    A successful Senior RAQA Consultant should have:
    A degree in Life Sciences, Pharmacy, or a related field.
    Extensive knowledge of Regulatory Affairs and Quality Assurance within the healthcare industry (Experience in SaMD is essential)
    Experience in preparing and submitting regulatory submissions.
    A competitive salary
    Remote working

    If you're a dedicated and driven professional with a passion for improving patient lives through quality assurance and regulatory affairs, we encourage you to apply for the Senior RAQA Consultant position today.

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