Regulatory Affairs Officers X 2

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 filling, labelling updates, renewals, marketing authorisation transfers.Write the local modules (ex: 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, in particular good knowledge of EU procedures (DCP, MRP).Ability to multi-task.Ability to communicate with colleagues in global countries.Autonomy, multi-tasking abilities.For full job spec and discussion, email your CV to ****** or call Tina at +353 1 2784701.
Thornshaw Scientific is a division of the CPL Group www.thornshaw.com

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