Flexible Working
Learning & Development
Wellbeing

GMP Inspector

Salary €73,313 - €85,017 per annum
Location Hybrid
{Mergefield Value}
{Mergefield Value}

This is a Temporary, Full Time vacancy that will close in {x} days at {xx:xx} BST.

Reporting to a Senior Inspector, the Inspector assesses the compliance of manufacturers with EU Good Manufacturing Practice (GMP). The inspector evaluates the compliance of sites inspected, in Ireland and abroad, with the requirements of National legislation (in Ireland), European community directives, regulations and guidance.  These sites may include;

 

  • Manufacturers and distributors of medicinal products.
  • Manufacturers of investigational medicinal products.
  • Sites involved in the importation and / or storage of medicinal products.
  • Manufacturers of active pharmaceutical ingredients and certain excipients.
  • Quality control laboratories.
  • Office based sites involved in batch certification activities only.

 

The role involves inspecting, reporting and forming conclusions about the suitability of a site for the activities it is authorised for or for which it has sought authorisation. The Inspector provides technical information and advice to individuals and organisations both internal and external to the HPRA.

The content below represents a broad guideline for the role of Inspector. Some aspects may be subject to change in accordance with business needs.

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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