Regulatory Affairs Specialist

2 weeks ago


Dublin, Dublin City, Ireland CPL Full time
Job Description

Thornshaw Scientific, in collaboration with a global pharmaceutical company, have a new opportunity for a Regulatory Affairs Specialist to join the team. Key responsibilities include managing EU marketing authorisation dossiers and submissions, preparing and filing EU submissions, and writing local modules and administrative documents.

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.
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


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