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    • Oxfordshire, England
    • Negotiable
    • Posted about 19 hours ago

    Job title: Regulatory Affairs Manager, Global Publishing A Biopharmaceutical company in Oxfordshire are seeking a Regulatory Affairs Manager, Global Publishing to join their Regulatory Operations team. This role will be responsible for the preparation and publishing of documentation for commercial and development submissions to global health aut...

    • Oxfordshire, England
    • Negotiable
    • Posted about 19 hours ago

    Job title: Regulatory Affairs Senior Associate, Global Publishing A Biopharmaceutical company in Oxfordshire are seeking a Senior Associate, Global Publishing to join their Regulatory Operations team. This role will be responsible for the preparation and publishing of documentation for commercial and development submissions to global health auth...

    • Dublin, Republic of Ireland
    • Negotiable
    • Posted about 19 hours ago

    Job title: Global Regulatory Affairs Director, Paediatrics A well-known pharmaceutical company are seeking a Global Regulatory Affairs Director to work in their recently launched paediatric centre of excellent office in Dublin. This is an exciting opportunity to join HIV and Emerging Viruses Regulatory Affairs where you will provide global regul...

    • Oxfordshire, England
    • Negotiable
    • Posted about 19 hours ago

    Job title: Regulatory Affairs Associate Director, Global Labelling A Biopharmaceutical company in Oxfordshire are seeking a Regulatory Affairs Associate Director, Global Labelling. Reporting directly into the Head of Global Labelling, this role will be responsible for both technical and operational support within Labelling across global markets....

    • Oxfordshire, England
    • Negotiable
    • Posted about 19 hours ago

    Job title: Regulatory Affairs Manager, Labelling A Biopharmaceutical company in Oxfordshire are seeking a Regulatory Affairs Manager, Labelling to join their Operations team. This role will have responsibility for preparing labelling documents for submission and implementation globally. Responsibilities: Manage quality control over entire labell...

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