Senior Quality Specialist

Job Description

An exciting role for a senior quality specialist to join a growing team on a permanent basis. This company specializes in import services and licenses for veterinary medicine in Ireland and abroad.

The successful person will have minimal 5 years' experience working preferably in a regulated pharmaceutical or medical device industry with prior experience with the HPRA. You will have excellent knowledge and experience of quality management systems. This role is based in Carlow.

Responsibilities:

• Support the site quality manager to ensure maintenance and continuous improvement of GMP quality management system.
• Technical writing of PQMS documents to include document creation and updates.
• Process validation activities.
• Review and approve SOPs, master and executed batch documentation, protocols, and reports.
• Review documentation for incoming inspection of material and approval.
• Maintenance of suppler qualification system.
• Oversee change controls, deviations, CAPAs, and complaint programme.
• Support with internal and external audits.
• Annual product quality reviews.
• Participate in quality management review meetings.
• Quality risk management programme.
• Review batch paperwork for finished product release in line with the QP.
• Function as deputy for quality coordinator and quality manager as needed.

If this role is of interest, please 'apply now' or contact me on 021 2300 300 or at

Morgan McKinley is acting as an Employment Agency and references to pay rates are indicative.

BY APPLYING FOR THIS ROLE YOU ARE AGREEING TO OUR TERMS OF SERVICE WHICH TOGETHER WITH OUR PRIVACY STATEMENT GOVERN YOUR USE OF MORGAN MCKINLEY SERVICES.