Quality Coordinator

About the role

The Quality Coordinator will join Abbott's site quality team at the Carbury Point manufacturing facility in Sligo. Working an evening shift, the role focuses on maintaining product and quality compliance within a highly regulated nutrition and medical device environment.

Key responsibilities

• Perform in‑process and final sampling and testing of manufactured products.
• Coordinate in‑process work order file documentation.
• Operate and maintain the electronic document management system (EDMS).
• Provide assistance to various functions on quality, technical, documentation, or related issues.
• Support CAPA investigations and develop corrective and preventive action plans.
• Assist with internal and supplier audits.
• Collect and report quality metrics as required.

Required profile

• Experience in product and quality compliance within a manufacturing setting.
• Willingness to work the specified evening shift schedule.

Required skills

• Proficiency with an electronic document management system.
• Knowledge of CAPA (Corrective and Preventive Action) processes.
• Familiarity with audit procedures and documentation.
• Ability to conduct sampling and testing of products.