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Executive Pharmaceutical Assessor, Pharmaceutical Assessment – Veterinary Sciences / Measúnóir Cógaisíochta Feidhmiúcháin, Measúnú Cógaisíochta - Na hEolaíochtaí Tréidliachta

Salary €85,300-€107,662
Location Hybrid
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This is a Temporary, Full Time vacancy that will close in {x} days at {xx:xx} BST.

 

Reporting to the Pharmaceutical Assessment Manager the role of the Executive Pharmaceutical Assessor is to in conjunction with their peers proactively participate in the management, development and operation of the Pharmaceutical Assessment section.

 

The Executive Pharmaceutical Assessor will achieve this through the following key aspects:

  • Management of personnel assigned to them by assisting the Pharmaceutical Assessment Managers in defining objectives, settings targets, coordinating activities, agreeing priorities, developing team members, maintaining effective communication lines and ensuring that the required standards, policies and practices are in place for the pharmaceutical assessment of all application types received.
  • Peer review of assessment reports produced by the Pharmaceutical Assessment team to ensure appropriate quality and consistency.
  • Pharmaceutical assessment and preparation of assessment reports on data submitted for veterinary medicinal products which are the subject of new applications and variations which are handled via national, decentralised and centralised procedures, assessment of scientific advice requests and other procedure types as appropriate to ensure appropriate quality.
  • Assist the Irish members of the Committee for Veterinary Medicinal Products (CVMP) on any matters related to marketing authorisation procedures including participating in discussions at monthly CVMP meetings.
  • Management of systems and procedures to support pharmaceutical assessment of applications received and to optimise capacity utilisation.

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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