Thornshaw Scientific Recruitment
Job title:
Regulatory Affairs & Senior Regulatory Affairs Officer
Company
Thornshaw Scientific Recruitment
Job description
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 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 in 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 [email protected] or call Tina at +353 1 2784703. Thornshaw Scientific is a division of the CPL Group www.thornshaw.com
Expected salary
Location
Dublin
Job date
Fri, 17 Jan 2025 23:10:35 GMT
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