Director, Quality & Regulatory Affairs

  • Director, Quality & Regulatory Affairs

    Our client develops cutting edge medical device products focused on medical aesthetics. They are currently looking for a highly skilled  Director of Quality & Regulatory Affairs to oversee and provide direction for quality and manufacturing functions.


    Responsibilities:
    • Ensure all SOP's are followed and that deviations are investigated
    • Review testing results and ensure that products meet all quality requirements before distribution
    • Manage customer complaints and reject returned items
    • Ensure all vendors are in compliance with company standards
    • Review and update SOP's on a regular basis
    • Oversee any changes related to products, ingredients, documentation and manufacturing procedures
    • Approve product changes and ensure specifications are changed accordingly
    • Provide reports to management and regulatory teams
    • Other duties as required


    Qualifications:
    • University degree
    • 8+ years of Quality Assurance experience in the pharmaceutical, cosmetic or medical device industry
    • Experience managing teams
    • Experience in medical device manufacturing is a strong asset
    • Strong leadership skills
    • Excellent communication and interpersonal skills


    To apply, please submit your resume using the "Apply Now" button.


    We thank all interested applicants, however only qualified candidates will be considered.