Quality Professional

About the role

We are seeking a Quality Professional to support the delivery of compliant, high-quality products, processes and services within Abbott’s regulated manufacturing environment in Ireland.

Key responsibilities

• Ensure adherence to quality standards, policies and regulatory requirements, and escalate non‑compliance issues.
• Review and approve documentation, process orders and perform inspections of incoming materials.
• Apply risk‑management tools such as FMEA, investigate quality issues and complaints, and recommend solutions.
• Support quality‑related projects, identify process improvement opportunities and contribute to validation, design‑control and change‑control activities.
• Collaborate with engineering, operations and suppliers, provide guidance to technicians and junior staff, and participate in audits and business initiatives.

Required profile

• Third‑level qualification in Life Sciences, Engineering or a related discipline.
• Minimum three years of experience in a quality or regulated environment.
• Strong understanding of quality systems and regulatory requirements.
• Proven ability to drive continuous improvement and support business objectives through quality excellence.

Required skills

• FMEA (Failure Mode and Effects Analysis)
• Validation activities
• Design controls
• Change control processes
• Quality Management Systems
• Risk management

What we offer

• Dynamic, regulated manufacturing environment.
• Opportunity to contribute to products that improve patients’ lives worldwide.
• Career development in quality and operational excellence.