Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio spans diagnostics, medical devices, nutritionals, and branded generic medicines. Abbott operates in more than 160 countries with 115,000 colleagues.In Ireland, Abbott has operated since 1946, employing over 6,000 people across ten sites, including manufacturing facilities and support operations in Clonmel, Cootehill, Donegal, Longford, Sligo, Dublin, and Galway. Abbott Ireland Diagnostic Division – Longford plays a vital role in meeting global demand for diagnostic testing in infectious disease, cancer, thyroid, and cardiovascular diseases.The Longford facility is located in Ireland’s midlands near the River Shannon, Lough Ree, and the Royal Canal, offering a vibrant community with a wide range of amenities and activities.Primary FunctionThe Manufacturing Manager is responsible for ensuring that the Longford facility meets customer, regulatory, financial, and safety goals through effective management of manufacturing and testing operations. This role supports new product and process transfers and leads strategic change initiatives to drive continuous improvement across the site.Key ResponsibilitiesLead and manage assigned manufacturing and support functions within OperationsEnsure major projects are delivered on time and within budgetMaintain product availability and meet customer requirements for diagnostic reagentsDrive timely completion of non-conformance investigations and CAPA activitiesPromote a culture of continuous improvement in safety, quality, and performanceOptimize human resources through effective communication, teamwork, and engagementEnsure compliance with GMP, HR, safety, financial, and quality proceduresStay current with technical and manufacturing developments to maintain regulatory complianceManage collaboration between Longford Operations and other Abbott sitesEnsure quality standards are met for internal and external audits and customer expectationsSupport strategic planning and execution of operational changesMaintain operational task lists and project plans (e.g., ETMS TO DO LIST)Conduct business in compliance with EHS laws and Abbott global standardsSupervisory / Management ResponsibilityDirect supervision and leadership of manufacturing teamsResponsible for team performance, development, and motivationEducation & ExperienceA relevant third-level qualification (e.g., Engineering, Science, or related discipline)Minimum 5 years’ experience in a regulated manufacturing environment (Medical Device or Diagnostics preferred)Minimum 3 years’ experience in people management and team motivationStrong communication and problem-solving skillsFamiliarity with regulatory requirements and quality systemsAccountabilityAccountable for the performance and compliance of assigned operationsDecision-making within agreed product availability and performance goalsOperates with general guidance from senior managementAnnual goals and performance reviews conducted with the Site Director
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