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    Excelya

    Biotechnology

    Vigilance Quality & Compliance Lead

    Paris, FranceHybridFull-timePosted 2mo ago
    All Excelya jobs

    Job description

    At Excelya, taking audacious steps is encouraged, so we’re looking for individuals who are ready to grow with us and share our values.   Master's degree in Pharmacy, Life Sciences, Quality Management, or a related field. Significant experience in Quality Assurance within the pharmaceutical, medical device, cosmetics, or healthcare industry. Strong knowledge of Pharmacovigilance, Materiovigilance, Cosmetovigilance, and applicable regulatory requirements.

    Solid understanding of GVP, GMP, ISO standards, health authority expectations, and quality systems. Experience managing audits, regulatory inspections, and quality oversight of external partners. Proven leadership and people management skills, with the ability to develop high-performing teams. Strong analytical, problem-solving, and continuous improvement mindset. Excellent stakeholder management, communication, and influencing skills in a cross-functional environment.

    Ability to manage multiple priorities in a complex and regulated environment. Fluent in English, French At Excelya, driven by Audacity, Care, and Energy, we invite you to join our team as a Vigilance & Compliance Manager. This role focuses on overseeing QA Vigilance & Compliance activities, ensuring regulatory compliance, quality oversight, and continuous improvement across vigilance processes. As a Compliance & Vigilance Manager you will be responsible to manage the Quality Assurance (QA) Vigilance and Compliance team for the Medical Care.

    Your

    Main responsibilities:

    • Lead and manage the QA Vigilance & Compliance team.
    • Define and implement quality and compliance requirements across vigilance activities.
    • Ensure compliance with applicable regulations, standards, and internal procedures.
    • Provide quality oversight and support for vigilance processes and documentation.
    • Manage third-party quality activities and coordinate internal and external audits.
    • Oversee compliance processes and KPI monitoring for regulatory safety reporting.
    • Support regulatory inspections and partner audits (ANSM, FDA, etc.).
    • Promote quality culture, continuous improvement, and regulatory intelligence.
    • Why Join Us?
    • At Excelya, we combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare.
    • Here’s what makes us unique.
    • We are a young, ambitious health company representing 900 Excelyates, driven to become Europe’s  leading mid-size CRO  with the  best employee experience .
    • Our  one-stop provider service model  offering full-service, functional service provider, and consulting enables you to evolve through diverse projects.
    • Working alongside preeminent experts, you will help improve scientific, operational, and human knowledge to enhance the patient’s journey.
    • Excelling with care  means benefiting from an environment that values your natural talents, pushes boundaries with audacity, and nurtures your potential, allowing you to contribute fully to our shared mission.

    Job details are sourced from the employer's original posting.

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    About the company

    Excelya

    Excelya is a company involved in in vitro applications, data flows, and quality control within the VITRO product domain. They focus on functional testing, data integrity, and documentation for deployments.

    View all Excelya jobs
    Industry
    Biotechnology
    Open roles
    32

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