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)
- Maintain and manage QMS documentation to meet regulatory standards.
- Write and review SOPs to ensure compliance and clarity.
- Support internal audits, CAPA, and change control processes.
- Track and report quality metrics to site leadership.
- Work cross-functionally to support QA activities and improvements.
- Identify and implement process improvements within the QMS.
- Ensure timely, accurate, and compliant QA documentation updates.
Knowledge, Skills and Experience Required for the Role:
- Degree in Science, Engineering, Quality, or related field.
- 1+ year’s experience (including placement) in a regulated or medical device environment.
- Good understanding of QMS principles and document control.
- Skilled in root cause analysis and problem-solving.
- Strong organisation, communication, and time management skills.
- Proficient in Microsoft Office and ERP systems.
For a confidential discussion and more information on the role contact Courtney Russell
courtney.russell@collinsmcnicholas.ie
+353 (0) 71 9108062