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Global Labelling Technical Regulatory Affairs Lead (Associate Director) Cork Not Disclosed
Senior Director Global Regulatory Lead Early Clinical Development Cork Not Disclosed
Associate Director Clinical Regulatory Scientist Cork Not Disclosed
Principal Scientist Global Regulatory Affairs CMC Cork Not Disclosed
Senior Regulatory Affairs Specialist EU Not Disclosed
Senior Regulatory Affairs Specialist EU Not Disclosed
Senior Regulatory Affairs Specialist EU Not Disclosed
Principal Scientist Global Regulatory Affairs CMC Limerick Not Disclosed
CMC Regulatory Principal Scientist Cork Not Disclosed

Regulatory Affairs Manager Career Profile

Regulatory Affairs Manager


This role is normally suited to someone with a minimum of 5 years in a Regulatory setting, ideally more. Management, departmental budgeting, training are some of the keys tasks involved on the non-technical side of the role.

Key Responsibilities

  • Coordinating, compiling and submitting Marketing Authorisation variations for existing approvals
  • Composing and reviewing Pre-IND information packages and NDA packages for registration of prescription products in the US through the FDA
  • Liaise with partner companies as the primary Regulatory Affairs contact for the company to achieve product registration in all new worldwide regions within projected timeframes
  • Regulatory Affairs European project team leader for all new projects
  • Interpreting EU and US regulatory guidelines and procedures and ensuring the regulatory compliance of the company in all new regions Establish and analyse department budget
  • Identify and recommend areas for cost savings from and Regulatory and compliance perspective
  • Provide Regulatory advice and feedback for all internal company departments and external partners
  • Maintain and apply a high level of awareness and understanding of the impact of existing and future planned regulations

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