At LEO Pharma Cork, quality is more than compliance - it is how we protect patients, strengthen trust and ensure that critical medicines are delivered with confidence. As our new Quality Specialist, you will play a central role in supporting API Manufacturing, driving thorough assessment of regulatory, validation, patient safety and product impact', robust quality processes and ensuring investigations are handled with precision, clarity and impact.At LEO Pharma, we are global leaders in medical dermatology and Critical Care, with 117 years of experience in bringing innovation to healthcare. Each year, close to 100 million people have a better day because of our medicines.In Cork, you will join a site with a clear purpose: supporting high-risk patient groups and critical-care conditions through high-quality medicines and continuous improvement.Your RoleAs our new Quality Specialist, you will provide essential site support to ensure compliance with the LEO Quality Management Systen, cGMP and applicable regulatory requirements. You will support batch release activities, strengthen quality documentation and play a key role in Deviations, Change Controls and Laboratory Investigations - ensuring issues are understood, communicated and resolved effectively.This is a broad and influential role where technical quality expertise, structured thinking and clear, confident communication are equally important
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