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Assessor - Medicine Shortages & Borderline Classification - Compliance/Measúnóir - Ganntanais Leighis & Aicmiú Teorann - Comhlíonadh

Salary €76,282 - €88,460 per annum
Location Hybrid
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This is a Temporary, Full Time vacancy that will close in {x} days at {xx:xx} BST.

The Assessor will work as part of a dynamic team within the Medicine Shortages and Borderline Classification (MSBC) section of the Compliance Department of the HPRA. They will be responsible for overseeing the coordination and management of human medicine shortages, their evaluation and outward communication. The role focuses on the prevention and mitigation of actual and potential medicine shortages, and will also involve working collaboratively across regulatory, industry and healthcare sectors.

 

The Assessor will be responsible for coordination of shortages nationally and is expected to contribute to ongoing enhancements of the national Medicine Shortage Framework (MSF). The Assessor will also actively support the HPRA’s contribution to the European Medicine Agency working parties on shortages as well as other EU institutions, where relevant.

 

Reporting to the MSBC Manger, the role of the Assessor is to support the MSBC section with these principal activities:

  • Reviewing and assessing notifications of potential or confirmed medicine shortages submitted by marketing authorisation holders.
  • Determine the potential impact on public health and collaborate with all parties necessary for the management of shortages, when they occur.  
  • Liaise with pharmaceutical companies, healthcare professionals, and other relevant stakeholders to ensure effective communication and management of shortages, including identifying and contributing to effective mitigation measures.
  • Contribute to the development of the HPRA’s shortage management systems and procedures.
  • Participate in national and EU-level working groups to align on strategies and implement best practices for both shortage prevention and management.

 

The position may be suitable for an individual with a pharmacy, medical, or public health-related background. Candidates should have a demonstrated ability for technical scientific report writing. The ideal candidate would have clinical experience, in particular in medicines management or similar discipline.

We are the Health Products Regulatory Authority (HPRA) and we regulate medicines and devices for the benefit of people and animals. We are committed to excellence in health product regulation through science, collaboration and innovation.

Our remit and regulatory functions include human and veterinary medicines, clinical trials, medical devices, controlled drugs, blood and blood components, tissues and cells, and cosmetic products.

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