This global healthcare company is committed to improving the health and well-being of people all over the world by developing, producing, and providing innovative healthcare services and solutions in more than 110 countries globally. With more than 30,000 employees in 30 countries around the world, this biopharmaceutical leader improves the lives of patients who suffer from many chronic, rare, prevalent, and sometimes life-threatening diseases.With a significant R&D pipeline and a diverse commercialised product portfolio in therapy areas such as immunology, hepatology, and intensive care to name but a few, this organisations has increased its investment in Ireland year on year, in addition to the widened scope of roles positioned at its operation in Dublin, which is a state of the art biologics manufacturing plant and one of the premier sites in Dublin.With its continued expansion in Ireland and internationally, a need has arisen in the organisation for aQuality Compliance Supervisorto lead the site's QA Compliance function at this growing site, at an opportune time to join the business.ResponsibilitiesSafeguard the consistent delivery of high-quality work that is always inspection-ready and compliant with both internal standards and external cGxP expectations.Uphold full compliance with GMP, EU Annex 1, FDA, and all other relevant regulatory and quality guidelines.Support cross-functional teams to achieve timely batch certification by ensuring all required documentation from the QA Compliance team is complete, accurate, and finalized within agreed timelines.Develop and track inter- and cross-team KPIs to measure performance against departmental goals and align outcomes with broader company objectives.Ensure team members are fully trained and capable across all functional responsibilities.Design and deliver internal and external training programs to strengthen both quality and technical expertise.Serve as the primary QA Compliance contact within the team, ensuring effective communication and distribution of compliance-related information.Represent QA Compliance in cross-functional discussions and deputise for other QA functions or the QA Manager when required.Lead and manage the QA Compliance team through coaching, mentoring, and performance management.Set clear objectives, support professional development, and guide the team toward operational excellence.Managing the full lifecycle of deviations, investigations, and CAPAs, ensuring data integrity and the robustness of quality systems.Conducting regular GEMBA walks and on-site audits across manufacturing and quality control areas.Performing internal audits within QA, QC, Validation, and Manufacturing functions.Build strong partnerships with QA, Manufacturing, and other key stakeholders to maintain alignment with quality compliance standards.Foster a LEAN mindset and encourage a proactive approach to continuous improvement. Support initiatives that reinforce a strong 'Quality Culture' throughout the organization.Provide ongoing feedback to team members to support their growth, maintain transparency, and nurture an open, collaborative workplace culture.ExperienceMinimum of 5 years of experience within the pharmaceutical or biopharmaceutical industry.Proven experience working in an aseptic manufacturing or product filling environment is highly desirable.Background in terminal filtration, drug substance, or drug product operations may be considerable.Demonstrated leadership or stakeholder management experience is essential.Established track record in deviation and CAPA management, with the ability to drive investigations to effective closure.Demonstrated decision-making capability, with the confidence to implement process improvements and quality-driven changes where required.To learn more about this role apply online or contact Treasa Prior at HRM on for a confidential discussion.