Abbott is seeking a Laboratory Technician for their Diabetes Care site in Kilkenny, Ireland. The successful candidate will perform a variety of sampling activities, conduct dosimetric analysis, and ensure compliance with regulatory standards. A third level qualification in Science or Manufacturing and two years of relevant experience are preferred. The role requires attention to detail, as well as the ability to maintain high-quality records. Join Abbott, an equal opportunities employer, and contribute to impactful work in the healthcare industry. #J-18808-Ljbffr
About Abbott Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 107,000 colleagues serve people in more than 160 countries. Abbott serves the Irish market with a diverse range of healthcare products including diagnostics, medical devices and nutritionals products. In Ireland, Abbott employs over 6000 people across tensites. We have seven manufacturing facilities located in Clonmel, Cootehill, Donegal, Kilkenny, Longford and Sligo and a third-party manufacturing management operation in Sligo. Abbott has commercial, support operations and shared services in Dublin and Galway. We have been operating in Ireland since 1946. Abbott Ireland Vascular Division Clonmel Abbott Vascular is one of the world's leading vascular care businesses. Abbott Vascular is uniquely focused on advancing the treatment of vascular disease and improving patient care by combining the latest medical device innovations with world-class pharmaceuticals, investing in research and development and advancing medicine through training and education. Our broad line of vascular devices–which includes vessel closure, endovascular and coronary technologies–are used to treat vessel diseases of the heart, carotid arteries and peripheral blood vessels. These vessel diseases can lead to heart attack, stroke, critical limb ischemia and other serious vascular conditions. Purpose of the Job With general guidance from functional management, responsible for providing team leadership to a group of employees committed to increased quality and productivity. Supports demand of the business unit. Identifies and analyses problems, plans tasks and solutions. Provides guidance to team on development, performance and productivity issues. Reports to functional and/or organisation management on team accomplishments, achievements and productivity. Shift pattern Monday to Friday (A/B shift - days and evenings) As a Production Supervisor, your key responsibilities will be as follows Implement a staffing plan by identifying resource requirements and coordinating with Operations Management and Planning Schedulers Monitor daily work operations and provide support to team members Develop your team through training and assigning progressively more challenging tasks Develop feasibility and execute continuous improvement projects to improve efficiency or remove waste from the process. Interact with key stakeholders: Quality, Engineering, Human Resources, Supply Chain, EHS, Operations Management, Finance & Operations Excellence. Monitor compliance with company policies and procedures Develop work schedule for department by assessing priorities, workload and available resources Education and Skills Level 7 qualification (full credits) and related work experience. We would be keen to speak with you if you have prior people management experience We offer Competitive salary and benefits package Opportunities for advancement and professional development : We take pride in filling many of our open roles internally through planned development processes. A supportive and inclusive work environment where your contributions are valued. Access to the best-in-class peer groups, leading technology and resources to support your success. Join a company that is committed to making a positive impact in the community and beyond. Potential career path We are looking for people who want to grow their careers with us. High-performing Production Supervisors will be encouraged to take opportunities that present themselves in other functions. We thrive on people gaining broad experience across our business, and the majority of our leadership team have been Production Supervisors on-site earlier in their careers. Process/Manufacturing Engineering, Quality, Operations Leadership, Supply Chain Planning & Purchasing, Equipment Engineering, Laboratory, Finance to name a few are always on the lookout for talented leaders with a proven ability to deliver in our Production environments. At Abbott, we are committed to fostering an inclusive workplace where everyone’s contributions are valued and respected. We believe that diversity is our strength, and we are committed to creating an inclusive workplace where everyone feels empowered to succeed. #J-18808-Ljbffr
A global healthcare leader in Ireland is seeking a Production Supervisor to provide team leadership and improve productivity in a dynamic environment. In this role, you will implement staffing plans, monitor operations, and develop your team through training and challenging tasks. The ideal candidate has a Level 7 qualification and prior people management experience. Join a company that values diversity and focuses on positive community impact. #J-18808-Ljbffr
Overview Abbott Clonmel, County Tipperary, Ireland Join to apply for the Sterilisation Manager role at Abbott . Abbott is a global healthcare leader with a portfolio spanning diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. About Abbott in Ireland Abbott has been operating in Ireland since 1946 and serves the Irish market with a diverse range of healthcare products. In Ireland, Abbott currently employs about 6,000 people across ten sites located in Dublin, Donegal, Clonmel, Cootehill, Galway, Kilkenny, Longford and Sligo. Connect with us at www.abbott.com and on LinkedIn, Facebook, Instagram, X and YouTube. Purpose Statement Sterilisation Manager is responsible for compliance with applicable Corporate and Divisional Policies and procedures. Key Responsibilities Leads team that conduct sterilization qualification for new products and/or changes to existing products. Leads team that performs sterilization validation for radiation sterilized products including dose setting and quarterly dose audits. Leads team that performs sterilization validation for ethylene oxide sterilized products including new product qualification, annual revalidations, residual EO studies, and D-value studies. Leads team that provides product development and Operations teams sterilization Subject Matter Expert support. Leads team that assists in Supplier Quality audits of contract sterilization facilities and third party manufacturers. Leads team that conducts dose audit failure investigations. Leads team that conducts Ethylene Oxide Biological indicator sterility positive investigations. Education Bachelor's degree plus 9+ years of related work experience with a strong understanding of the specified functional area, or an equivalent combination of education and work experience. Advanced degree preferred. Experience Substantial knowledge of a Radiation and/or Ethylene Oxide or other sterilization modality. Uses in-depth knowledge of business unit functions and cross group dependencies/relationships. Recognized as an SME in work group and across functions. Ability to lead a technical team in the execution of sterilization validation/revalidation, new product qualification, troubleshooting sterilization issues. Will lead team performing this job in a quality system environment. Failure to adequately perform tasks can result in noncompliance with governmental regulations. Works on problems where analysis of situations or data requires an in-depth evaluation of various factors. Exercises judgment within broadly defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining results. Has broad knowledge of various technical alternatives and their potential impact on the business. Seniority level Mid-Senior level Employment type Full-time Job function Other Industries Hospitals and Health Care Referrals increase your chances of interviewing at Abbott by 2x #J-18808-Ljbffr
Laboratory Technician – Abbott Diabetes Care Kilkenny We currently have a requirement for a Laboratory Technician to join our New Abbott Diabetes Care Kilkenny site. Pre‑employment medical examination, including drug and alcohol screening, is required. Any offer of employment is conditional upon successful completion of this exam. Major Responsibilities Perform a variety of sampling activities to support product manufacture in a cGMP regulatory environment. Perform dosimetric analysis, dose map execution and equipment maintenance, in accordance with GLP, GMP and ISO 11137. Ensure that all work carried out is in compliance with the required regulatory standards, conforms to company policies and standard operating procedures (SOPs). Assist in the design and set‑up of the site dosimetry lab program. Create and update documentation as needed. Support the set up and maintenance of laboratory equipment and consumables. Ensure the laboratory is adequately stocked and resourced, with everything accurately labelled. Participate in validation activities as needed for dosimetry lab and equipment qualification program. Review and approve laboratory test results. Complete records on time and review data for accuracy and completeness. Assist in the identification of root cause analysis and provide technical advice as needed. Support unplanned events and raise out‑of‑specification results in a timely manner and inform the Supervisor immediately of any such events. Initiate and complete CAPAs and change controls in accordance with site procedures. Trend data for environmental and product monitoring, and generation and presentation of quarterly and annual reports. Maintain a “right first time” approach to quality records by ensuring accountability for functional responsibilities. Education & Experience Third level Science / Manufacturing or equivalent qualification. Preferred: two years’ work experience in a Manufacturing / Science / Quality or equivalent environment. Electron beam or other sterilisation technologies experience desirable. Knowledge in ISO 11137 desirable. Chemistry/Microbiology/Dosimetry Lab experience desirable. Equal Opportunity Employer Abbott is an equal opportunities employer. #J-18808-Ljbffr
About Abbott Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life‑changing technologies spans diagnostics, medical devices, nutritionals, and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries. Opportunity This position works out of Abbott’s Galway site within the Informatics Division of Abbott Rapid Diagnostics. Abbott empowers smarter medical and economic decision‑making. More than 10 million tests are run daily on Abbott diagnostics instruments worldwide. As a Global Product Manager , the role bridges customer needs with innovative solutions that enhance client and patient experiences. Responsibilities include leading product strategy, roadmap planning, execution, and stakeholder management for next‑generation software products. What You’ll Work On Conduct market research, competitor analysis, and gather customer feedback Benchmark best‑in‑class competitors and emerging technologies Collaborate with stakeholders to gather, analyze, and understand Voice of the Customer Support Product Manager with internal and external discovery sessions Execution Oversee product GTM activities in partnership with Product Manager Support Intranet and Website content management Lead the development of partner and distributor‑focused marketing Foster strong relationships with internal and external stakeholders Participate in industry events and speaking engagements Partner with US and Strategic Marketing and Sales on training materials, sales tools and campaign development Product Performance Analysis Define KPIs and success metrics Analyze data and user feedback to evaluate performance Identify improvement opportunitiesPrepare regular performance reports and executive presentations Compliance Complies with regulatory requirements, company policies, and operating procedures Maintains positive and cooperative communication with employees, customers, contractors, and vendors Required Qualifications Bachelor’s degree in Business, Marketing, Information Technology, Computer Science, Engineering, Data Science, or related field (Master’s preferred) 10 years of experience in Marketing, material development, storytelling, working with agencies, creating reporting and tracking, tactical plan and multichannel marketing experience. Understanding of PPC, Google Analytics, SEO. Reporting and copywriting expertise. Proven success managing IT/software products end‑to‑end Ability to travel up to 10% Preferred Qualifications Strong multitasking and prioritization skills Excellent organizational and problem‑solving abilities Strategic thinking with execution focus Strong presentation skills for diverse audiences Experience with product documentation, release notes, and training materials Budget and agency management experience #J-18808-Ljbffr
Abbott is seeking a Global Product Manager for its Galway site. The role focuses on bridging customer needs with innovative solutions in product strategy and execution. Key responsibilities include market research, product management, and compliance with regulatory standards. The ideal candidate has a Bachelor's degree in a relevant field and at least 10 years of experience in marketing or product management. Abbott offers a dynamic environment with opportunities for professional growth and development. #J-18808-Ljbffr
Purpose of the Role The Lead, Calibration & Analytical Lab is responsible for leading and overseeing analytical laboratory setup and calibration activities, ensuring full compliance with GMP, regulatory requirements, and internal quality standards. This role manages the analytical and calibration functions and associated personnel to achieve departmental and site objectives, while providing strong technical leadership, operational oversight, and continuous improvement across services that support ADC and its customers. Responsibilities Lead and oversee analytical laboratory setup activities, ensuring adherence to GMP, regulatory, and internal quality standards. Manage the Analytical and Calibration departments, including personnel, systems, and daily operations, in alignment with site and departmental goals. Act as the site Subject Matter Expert (SME) for analytical laboratories, calibration systems, and Maximo, supporting internal and external audits. Manage the site Maintenance and Calibration Management System (Maximo) and associated assets, including authorisation of system changes. Provide technical leadership for analytical test method transfers and the setup of new analytical laboratory spaces. Ensure compliant control of production, inspection, measuring, and test equipment across the site. Liaise cross‑functionally and divisionally as technical lead for site projects, ensuring alignment with timelines and strategic objectives. Procure laboratory equipment and consumables based on forecasted requirements, site needs, and budget constraints. Negotiate, manage, and maintain contracts and relationships with external calibration and analytical service providers. Ensure quality and compliance issues are promptly identified, investigated, and addressed through effective corrective and preventive actions. Lead and manage departmental activities during audits and represent the site as SME where required. Oversee periodic review of procedures to ensure ongoing compliance and alignment with business needs. Manage departmental budgets, approve purchases and invoices, and control expenditure within defined limits. Support onboarding, training, performance management, and career development of team members, fostering a strong culture of quality and continuous improvement. Promote and manage Health & Safety within the department, proactively reducing risk and reinforcing shared accountability. Ensure accurate, timely, and reliable data reporting to Site, Division, and Corporate management to support quality and business decisions. Education And Experience NFQ Level 7 qualification or higher in Engineering, Science, or a related discipline. Minimum of 4 years’ experience managing calibration system requirements within the medical device and/or pharmaceutical industry. Proven experience operating in a regulated GMP environment, including audit participation and quality system management. Demonstrated ability to lead teams, manage complex technical operations, and drive continuous improvement initiatives. What We Offer Attractive compensation package that includes competitive pay. Family health insurance. Excellent pension scheme. Life assurance. Career Development. Fantastic new facility. Growing business plus access to many more benefits. Abbott is an equal opportunities employer. #J-18808-Ljbffr
Abbott in Kilkenny is seeking a Lead for Calibration & Analytical Lab to oversee laboratory setup and calibration activities. The role requires strong leadership and technical expertise to ensure compliance with GMP and regulatory standards. You will manage the analytical and calibration functions, support audits, and drive continuous improvement initiatives. Candidates should have a NFQ Level 7 qualification in Engineering, Science, or related fields and a minimum of 4 years of relevant experience. Attractive compensation and benefits included. #J-18808-Ljbffr
About Abbott Abbott is a global healthcare company creating life‑changing technologies used by people around the world. Our Abbott Diabetes Care site in Kilkenny is a modern manufacturing facility producing FreeStyle glucose test strips and sensors. About The Role As a Manufacturing Line Operator, you will work on the production floor in a regulated, process‑driven environment, supporting daily manufacturing schedules while following strict quality and safety standards. This role suits someone who is : Comfortable with hands‑on, routine production work Reliable, detail‑focused and safety‑conscious Happy working to defined procedures and schedules What You’ll Do Operate production and/or test equipment Follow GMP, safety rules and standard operating procedures Meet daily production targets with guidance from your Supervisor Record production data accurately using approved systems Perform basic troubleshooting and elevate issues as required Support training of new team members when needed Contribute to continuous improvement activities What We’re Looking For Manufacturing or production experience is an advantage, but not essential Good communication and teamwork skills Basic computer skills A positive, flexible attitude and strong attention to detail Experience in regulated or manufacturing environments (e.g. medical device, pharma, food, automotive) is beneficial. What We Offer Competitive pay Health insurance Excellent pension scheme Life assurance Career development opportunities Fantastic new facility in a growing business Please note: Any offer of employment is conditional on successful completion of a pre‑employment medical, including drug and alcohol screening. Abbott is an equal opportunities employer. #J-18808-Ljbffr
