Regulatory Affairs Officer & Senior Regulatory Affairs Officer
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.
Minimum Requirements:
* 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
Seniority Level
Entry level
Employment Type
Full-time
Job Function
Legal
Industries
Staffing and Recruiting
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