Excellent opportunity for a Quality Systems Specialist to join a Medical Devices company in Galway. The Quality Systems Specialist will maintain and improve the Quality Management System to ensure strong compliance, documentation control, and product quality. Ideal for a recent graduate looking to build a career in Quality Assurance within the medical device industry, with hands-on exposure to key quality processes and cross-functional teamwork.
Overview of your responsibilities (full job description available on request)
1. Maintain and manage QMS documentation to meet regulatory standards.
2. Write and review SOPs to ensure compliance and clarity.
3. Support internal audits, CAPA, and change control processes.
4. Track and report quality metrics to site leadership.
5. Work cross-functionally to support QA activities and improvements.
6. Identify and implement process improvements within the QMS.
7. Ensure timely, accurate, and compliant QA documentation updates.
Knowledge, Skills and Experience Required for the Role:
8. Degree in Science, Engineering, Quality, or related field.
9. 1+ year's experience (including placement) in a regulated or medical device environment.
10. Good understanding of QMS principles and document control.
11. Skilled in root cause analysis and problem-solving.
12. Strong organisation, communication, and time management skills.
13. Proficient in Microsoft Office and ERP systems.