As a Quality Assurance Specialist-Validation you'll be the go-to expert ensuring processes, equipment, and facilities meet the highest GMP and regulatory standards in this biologics manufacturing company in Sligo. What You'll Do: Be the QA expert for validation activities, guiding strategies, resolving issues, and ensuring compliance. Review and approve validation documents for facilities, equipment, and utilities. Manage Quality Management System (QMS) areas like deviations, change controls, CAPAs, audits, and vendor management. Collaborate with cross-functional teams to support new product introductions and continuous improvements. Apply risk assessment tools (like FMEA) to ensure robust processes. Keep projects on track by meeting timelines for GMP and validation reviews. What You'll Bring: A degree in science or engineering. 5+ years' experience in a GMP quality role with a strong focus on validation. Solid understanding of validation processes, project life cycles, and cGMP regulations. A proactive, problem-solving mindset and strong teamwork skills. Why Join ? Be part of a team that's shaping the future of manufacturing. Work in a cutting-edge facility with opportunities to grow. Competitive salary and benefits package/opportunity for hybrid work. A role where your expertise and ideas truly make a difference. Ready to Make an Impact? Apply now and take the next step in your QA career! Keywords: QA Specialist, Quality Specialist, Validation Specialist, Skills: Validation QA Specialist Quality Specialist Validation Specialist GMP Benefits: Benefits