Data Quality Specialist

Team Horizon is seeking an experienced quality professional with an information delivery background to join our client’s team in Dublin. This role requires a strong understanding of Pharmaceutical Quality Systems, data validation and data verification to support key business deliverables.

Why you should apply:

• Opportunity to offer support to a project and integrate diverse perspectives to add value to the achievement of team goals and timely decision-making.


• Hybrid role, 3 days on site

What you will be doing:

• Support the delivery of a Quality Management Review (QMR) project
  Support Information delivery across all business units using Power BI or other Data reporting and visualizations tools as required


• Support data validation and data verification activities, proactively identify data integrity issues and support corrective actions.


• Gather information from necessary business partners to create and monitor of Quality Systems metrics in compliance with internal and external requirements.


• Assist in the development of appropriate systems and processes to ensure delivery of information across function to support enhanced performance culture.


• Collaborate with stakeholders to identify and support value-added improvements and Key Performance Indicators (KPIs) to the QMR.


• Support procedural documentation and working practice document creation, update, and execution.


• Ensure compliance with GxP (Good Practice) guidelines and regulatory requirements in all documentation and quality systems activities.


• Maintain thorough and accurate GxP documentation to support compliance and inspection readiness.


• Triage report requests/issues related to QMR via our ticketing system.


• Provide forward thinking innovative solutions and identify opportunities to add value to the teams’ deliverables.


•  Other duties as required to support the growing Quality organization.

What you need to apply:

• 5+ years of experience in a Quality Systems role within the pharmaceutical industry and working to GxPs.


• Knowledge of requirements for a Quality Management System


• Experience in authoring, reviewing, and maintaining GxP documentation to ensure regulatory compliance


• Direct experience and comprehension of systems supporting pharmaceutical manufacturing, IT infrastructure, and/or laboratory operations.


• Prior experience in project leadership within a matrix environment.


• Business engagement skills, with the ability to partner with both technical and non-technical roles • Able to prioritize and manage workload and manage shifting priorities based on criticality to ensure commitments are met.


• Ability to work to tight deadlines


• Strong understanding of GxP guidelines and compliance requirements.


• Experience working in data warehouse building and administration