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  • Dublin, Dublin City, Ireland Cpl Full time

    Regulatory Affairs Officer & Senior Regulatory Affairs OfficerThornshaw Scientific, in collaboration with my client, a global pharmaceutical company, now have a new opportunity for a Regulatory Affairs Officer to join the Dublin team. The same company also have Senior Regulatory Affairs Officer opportunities.Key Responsibilities:Manage EU marketing...


  • Dublin, Dublin City, Ireland Cpl Healthcare Full time

    Thornshaw Scientific, in collaboration with my client, a global pharmaceutical company, now have a new opportunity for a Regulatory Affairs Officer to join the Dublin team.The same company also has Senior Regulatory Affairs Officer opportunities.Key Responsibilities:Manage EU marketing authorisation dossiers and submissions (MAAs, lifecycle activities,...


  • Dublin, Dublin City, Ireland Cpl Healthcare Full time

    Thornshaw Scientific, in collaboration with my client, a global pharmaceutical company, now has a new opportunity for a Regulatory Affairs Officer to join the Dublin team.The same company also has Senior Regulatory Affairs Officer opportunities.Key Responsibilities:Manage EU marketing authorisation dossiers and submissions (MAAs, lifecycle activities,...


  • Dublin, Dublin City, Ireland Cpl Healthcare Full time

    Thornshaw Scientific, in collaboration with my client, a global pharmaceutical company, now have a new opportunity for a Regulatory Affairs Officer to join the Dublin team. The same company also has Senior Regulatory Affairs Officer opportunities.Key Responsibilities:Manage EU marketing authorisation dossiers and submissions (MAAs, lifecycle activities,...


  • Dublin, Dublin City, Ireland Cpl Healthcare Full time

    Thornshaw Scientific, in collaboration with my client, a global pharmaceutical company, now has a new opportunity for a Regulatory Affairs Officer to join the Dublin team. The same company also has Senior Regulatory Affairs Officer opportunities.Key Responsibilities:1. Manage EU marketing authorisation dossiers and submissions (MAAs, lifecycle activities,...


  • Dublin, Dublin City, Ireland Cpl Healthcare Full time

    Thornshaw Scientific, in collaboration with my client, a global pharmaceutical company, now has a new opportunity for a Regulatory Affairs Officer to join the Dublin team. The same company also has Senior Regulatory Affairs Officer opportunities.Key Responsibilities:Manage EU marketing authorisation dossiers and submissions (MAAs, lifecycle activities,...


  • Dublin, Dublin City, Ireland Cpl Healthcare Full time

    Thornshaw Scientific, in collaboration with my client, a global pharmaceutical company, now have a new opportunity for a Regulatory Affairs Officer to join the Dublin team. The same company also has Senior Regulatory Affairs Officer opportunities.Key Responsibilities:1. Manage EU marketing authorisation dossiers and submissions (MAAs, lifecycle activities,...


  • Dublin, Dublin City, Ireland Cpl Healthcare Full time

    NEW OPPORTUNITY - Thornshaw Scientific, in collaboration with my client, a global pharmaceutical company, now have a new opportunity for a Regulatory Affairs Officer to join the Dublin team. Key Responsibilities: Manage EU marketing authorisation dossiers and submissions (MAAs, lifecycle activities, variations, transfer etc.)for our current portfolio of...


  • Dublin, Dublin City, Ireland Thornshaw Recruitment Full time

    Thornshaw Scientific, in collaboration with my client, a global pharmaceutical company, now have opportunities for Regulatory Affairs Officers to join the Dublin team.Key Responsibilities:Manage EU marketing authorisation dossiers and submissions (MAAs, lifecycle activities, variations, transfer etc.) for our current portfolio of pharmaceutical...


  • Dublin, Dublin City, Ireland Cpl Healthcare Full time

    NEW OPPORTUNITY - Thornshaw Scientific, in collaboration with my client, a global pharmaceutical company, now have a new opportunity for a Regulatory Affairs Officer to join the Dublin team.Key Responsibilities:Manage EU marketing authorisation dossiers and submissions (MAAs, lifecycle activities, variations, transfer etc.) for our current portfolio of...


  • Dublin, Dublin City, Ireland Thornshaw Scientific Recruitment Full time

    On behalf of my client, a global pharmaceutical company, we have a new vacancy for a Senior Regulatory Affairs Officer to join the team in Dublin. This is a permanent role with hybrid offering.Fantastic opportunity to join a fast-growing organisation with an exciting portfolio pipeline.The role & responsibilities:Manage marketing authorization dossiers and...


  • Dublin, Dublin City, Ireland Cpl Healthcare Full time

    On behalf of my client, a global pharmaceutical company, we have a new vacancy for a Senior Regulatory Affairs Officer to join the team in Dublin.This is a permanent role with hybrid offering.Fantastic opportunity to join a fast growing organisation with exciting portfolio pipeline.The role & responsibilities:Manage marketing authorization dossiersand...


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    On behalf of my client, a global pharmaceutical company, we have a new vacancy for a Senior Regulatory Affairs Officer to join the team in Dublin. This is a permanent role with hybrid offering. Fantastic opportunity to join a fast-growing organisation with an exciting portfolio pipeline.The Role & Responsibilities:Manage marketing authorization dossiers and...


  • Dublin, Dublin City, Ireland CPL Full time

    Thornshaw Scientific, in collaboration with my client, a global pharmaceutical company, now have a new opportunity for a Regulatory Affairs Officer to join the Dublin team. The same company also have Senior Regulatory Affairs Officer opportunities.Key Responsibilities:• Manage EU marketing authorisation dossiers and submissions (MAAs, lifecycle...


  • Dublin, Dublin City, Ireland CPL Full time

    Thornshaw Scientific, in collaboration with my client, a global pharmaceutical company, now have a new opportunity for a Regulatory Affairs Officer to join the Dublin team. The same company also have Senior Regulatory Affairs Officer opportunities.Key Responsibilities:• Manage EU marketing authorisation dossiers and submissions (MAAs, lifecycle...


  • Dublin, Dublin City, Ireland Cpl Healthcare Full time

    Job Description:Cpl Healthcare on behalf of their client, a global pharmaceutical company, is seeking a highly skilled Regulatory Affairs Manager to join their team in Dublin.This full-time/hybrid position reports to the Global Regulatory Affairs Associate Director and involves taking a lead role and responsibility for planning, executing, tracking, and...


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  • Regulatory Affairs

    3 weeks ago


    Dublin, Dublin City, Ireland Thornshaw Recruitment Full time

    Thornshaw Scientific, in collaboration with my client, a global pharmaceutical company, now have a new opportunity for a Regulatory Affairs Officer to join the Dublin team.Key Responsibilities:Manage EU marketing authorisation dossiers and submissions (MAAs, lifecycle activities, variations, transfer etc.) for our current portfolio of pharmaceutical...


  • Dublin, Dublin City, Ireland CPL Full time

    On behalf of my client, a global pharmaceutical company, we have a new vacancy for a Senior Regulatory Affairs Officer to join the team in Dublin. This is a permanent role with hybrid offering.Fantastic opportunity to join a fast growing organisation with exciting portfolio pipeline.The role & responsibilities:Manage marketing authorization dossiers and...

Regulatory Affairs Officers

1 week ago


Dublin, Dublin City, Ireland Cpl Healthcare Full time

Thornshaw Scientific, in collaboration with my client, a global pharmaceutical company, now have a new opportunity for a Regulatory Affairs Officer to join the Dublin team. Key Responsibilities: Manage EU marketing authorisation dossiers and submissions (MAAs, lifecycle activities, variations, transfer etc.)
for our current portfolio of pharmaceutical products.Prepare and file the EU submissions including life-cycle maintenance variations, initial MAA filing, labelling updates, renewals, marketing authorisation transfers.Write the local modules (e.g., module 1) and administrative documents.Compile regulatory documentation received from other departments (CMC, clinical) for DCP, MRP and national applications in line with assigned timelines (including responses to questions).Effective high-quality communication with European Regulatory Authorities, participate in meetings with health authorities as needed.
Follow-up of the submissions with HA.To be considered for this new opportunity you need to meet the following criteria: Life Science qualification.2-3 years of experience in Regulatory Affairs, particularly good knowledge of EU procedures (DCP, MRP).Ability to multi-task.Ability to communicate with colleagues in global countries.Autonomy and multi-tasking abilities.For full job spec and discussion, email your CV to ****** or call Tina or Linda at

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