This global pharmaceutical company employ a highly experienced international team focused on maximising the commercial potential of pharmaceutical products across Europe and other territories.
They boast a solid dose manufacturing and packaging facility in Dublin, a regulatory affairs and PV office located in Tipperary and a commercial office in the UK.
Due to continued growth and the increase in their product portfolio they seek a PV professional to join their operation in Tipperary.
Reporting to the director of Regulatory affairs and the QPPV, you will have responsibility across the following:
In order to qualify for the role you must possess the following in order to be considered:
To find out more apply online or call Gillian McMurrough directly on +353 1 6321827 to have a confidential discussion.