Pharmacovigilance Specialist (PV) – Part Time

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.

The Role

Reporting to the director of Regulatory affairs and the QPPV, you will have responsibility across the following:

  • Review and co-ordination of Safety Data Exchange Agreements
  • Oversee maintenance of the Pharmacovigilance System Master File (PSMF)
  • Writing and updating in-house Pharmacovigilance SOPs
  • Provision of information to pharmacovigilance service providers related to MAs
  • Reporting to QPPV to ensure QP oversight in relation to safety variations
  • Receipt and co-ordination of medical queries and ADRs

The Person

In order to qualify for the role you must possess the following in order to be considered:

  • A BSc in Science or related
  • 2+ years industry experience within a PV function
  • Knowledge and understanding of the EU regulatory framework related to pharmacovigilance activities
  • Eligible to work within EU?

The Benefits:

  • Excellent Training
  • Competitive salary
  • Healthcare
  • Pension

To find out more apply online or call Gillian McMurrough directly on +353 1 6321827 to have a confidential discussion.

Salary: On Application Location: Tipperary