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Good Distribution Practice (GDP) Inspector, Market Surveillance, Compliance / Cigire Dea-Chleachtais Dáileacháin, Faireachas Mhargaidh, Comhlíonadh

Salary €77,045-€89,345 per annum (incremental scale)
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 Good Distribution Practice (GDP) Inspections Manager, the GDP Inspector will be responsible for assessing the compliance of national operators involved in the pharmaceutical and chemical industries.  

The GDP Inspector will evaluate the compliance of sites against the requirements of national legislation, European Community Directives, Regulations and Guidance in the areas of GDP and Controlled Drugs or precursor chemical requirements. 

These sites may include:

  • Distributors of human medicinal products
  • Brokers of human medicinal products
  • Importers and distributors of active substances
  • Manufacturers, distributors and other entities utilising controlled drugs and precursor chemicals
  • Other inspection activities as may be required.

Inspectors require excellent communication skills, a high degree of flexibility and the ability to respond to changing priorities. They also provide technical information and advice to individuals and organisations both internal and external to the HPRA.

GDP inspectors inspect within Ireland only. On average most inspections are for one day on site and inspectors, once fully trained, usually perform six to eight inspections per month.  Full training is provided to all new inspectors. This role is being offered as part of our current hybrid working model.

The successful candidate will work closely with the other members of the GDP team and liaise effectively with the Licensing, Controlled Drugs, GMP inspection and Enforcement teams and any other sections of the HPRA that require support. 

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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