Closing date for applications: 23/10/2018
Reporting to a Senior Inspector, the Inspector will be primarily responsible for assessing the compliance of manufacturers with EU Good Manufacturing Practice (GMP).
The role of an Inspector is to evaluate 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;
o Manufacturers and distributors of medicinal products
o Manufacturers of investigational medicinal products
o Sites involved in the storage of medicinal products
o Manufacturers of active pharmaceutical ingredients and certain excipients
o Contract quality control laboratories
The Inspector provides technical information and advice to relevant individuals and organisations both internal and external to the HPRA and provide support to the enforcement and execution of national regulations in relation to medicinal products.
Role Profile Application Form