Overview
QAV Specialist - Ireland, Cork - 12 Months Initial Contract
Our client is undergoing major expansion, supported by substantial investment aimed at increasing its overall manufacturing capacity in the medical device sector.
Recent upgrades include the development of new, state-of-the-art facilities, advanced automation systems, and additional infrastructure enhancements designed to strengthen operational resilience and meet growing global healthcare demands.
With a long-established presence and a highly skilled workforce, the site requires the role of a QAV Specialist to join their project based in Cork.
What you'll do
Ensuring that the QAV/QC/QA deliverables are achieved in line with the project schedule.
Ensuring that the site and global procedures and processes are managed and adhered to while ensuring the ISPE Verification guideline for the project are followed.
Manage the co-ordination and workload of assigned deliverables for the QA stream.
Participate in equipment, process and/ or design FMEAs.
Provision of CSV compliance expertise and review and approval of CSV documentation.
What you'll need
3rd level qualification in a relevant Science/Engineering discipline, an advanced degree is preferred but not essential.
Extensive experience as a Quality SME in Qualification/ Validation projects within a regulated pharmaceutical environment.
Project management experience or experience being a key player in large capital expenditure projects is essential for this role.
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