CareerWise Recruitmentis seeking anEngineering Quality Engineerto join a leading multinational company based inCork. This is a12-month contract roleoffering ahighly competitive hourly rate.The successful candidate will act as aSubject Matter Expert (SME)in Engineering quality systems, documentation, and compliance processes. In this role, you will work closely with the Quality and Operations teams to strengthen quality documentation, improve compliance practices, and ensure all activities meet regulatory and corporate standards.Support the development and implementation of the site's Quality strategy and continuous improvement initiatives.Take ownership of Quality documentation systems, ensuring procedures, work instructions, and records are accurate, current, and compliant with regulatory standards.Review and update quality documentation to address gaps and ensure audit readiness.Lead or support internal and external audits, including preparation, coordination, and follow-up of findings.Partner with cross-functional teams to ensure quality and regulatory requirements are met in all manufacturing and process activities.Degree in a relevant Science or Engineering discipline (Quality, Manufacturing, Mechanical, Biomedical, etc.) or equivalent experience.Minimum of 3 years' experience in a regulated manufacturing or medical device environment.Strong experience in Quality Systems and Documentation Control (SOPs, CAPAs, NCRs, Change Control, etc.).Excellent understanding of ISO, FDA, and other relevant regulatory standards.