A leading healthcare company in Clonmel seeks a quality management specialist to oversee supplier performance, provide technical support, and drive process improvements. The ideal candidate has a relevant level 7 qualification and 2+ years of experience. Strong project management and supplier management skills are essential for this role, which offers an opportunity to influence quality standards and drive supplier performance improvements. #J-18808-Ljbffr
A global healthcare leader is seeking an Operational Excellence & Lean Specialist in Kilkenny, Ireland. This mid-senior level role focuses on driving continuous improvement initiatives, employing Lean Six Sigma methodologies, and collaborating with cross-functional teams to deliver measurable results. A Bachelor's degree and Lean Six Sigma Green Belt certification are required. Attractive compensation and benefits are offered. #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 113,000 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 6,000 people across ten sites. We have six manufacturing facilities located in Clonmel, Cootehill, Donegal, 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 Nutrition Division Cootehill Cavan Abbott Nutrition produces a range of infant formulae in all pack sizes under the brand name “Similac”. To complement the range of “Similac” infant formulae, the facility also manufactures a range of follow‑on formulae under the brand name of “Gain”. The essential ingredient is liquid skim milk and this is combined with carbohydrate, vegetable oils, vitamins and minerals. The product is blended, pasteurised, dried and packaged at the site and once packaged, is distributed to Europe, South East Asia, the Middle East, Latin America and Canada. Established in 1975, Abbott Nutrition in Ireland is the largest powder manufacturing facility for the production of infant formulae within the Abbott Corporation worldwide. Approximately 1,000 dairy farms in Ireland and Northern Ireland supply quality milk to the Cootehill facility which processes 500,000 litres per day. This secure supply together with Ireland’s reputation as a green, clean environment is of significant strategic importance to Abbott Nutrition. The Role of Materials Planner Purpose of the Job The Planner is responsible for detailed plant scheduling and coordinating the flow of information and product through the supply chain. The role is a key contact with important customers, with suppliers, with Abbott Distribution and also with other Abbott locations. Key Responsibilities Provide a planning function to ensure plant output aligns with market needs and agreed schedules through the supply chain. Offer backup expertise to other planning areas and support the Purchasing and Warehouse functions. Maintain accuracy in the inventory control system. Ensure effective management of Material Requirement Planning (MRP) and inventory. Ensure customer focus and product availability through effective MRP management, while maintaining cost and quality compliance. Continuously analyze MRP parameters (reorder point, minimum lot size, rounding values, etc.). Monitor inventories and address slow‑moving or obsolete stock. Schedule materials to meet plant operational requirements, ensuring efficient and effective purchasing practices. Collaborate with internal functional areas to ensure operational efficiency. Drive continuous improvement within the planning area to promote operational excellence and improve financial performance. Maintain local planning policies and procedures in line with overall Abbott requirements. Manage key metrics to measure performance against set targets, analyze data to support decision‑making, and report findings to the appropriate audience. Develop and grow relationships with other manufacturing sites, corporate teams, ANSC Purchasing, and ANSC Materials Management, as well as suppliers and other elements of the supply chain. Maintain records and files for key suppliers and assist in monitoring supplier performance against KPIs. Adapt to changes in job functions due to updates in GMP, EHS, technical/new equipment, quality procedures, and SOPs. Be adaptable and flexible to changing plant needs. Report to the Planning Manager within the overall Materials Management function. Work with ALOG (Planning Center) and supply chain members to meet target performance on KPIs, including customer service and inventory levels. Ensure compliance with local (including ISO) and Abbott rules, policies, and regulations, as well as all regulatory requirements (local and market‑specific). Provide data to support the development of the annual plan and product cost. Education & Experience Bachelor’s Degree: Appropriate qualification in either Purchasing/ Production Planning e.g. Diploma in Purchasing or relevant APICS (American Production and Inventory Control Society) examinations. Or General Degree with relevant Manufacturing experience. A minimum of 3 years experience within a regulated manufacturing environment. Previous experience in a planning or supply chain role is essential. Key Skills Excellent interpersonal skills and communication skills. Good team working skills are required but also the ability to work alone on own initiative. A high level of computer literacy is required. Good logic and computing capability is required. A high level of integrity is essential. The ability to handle complex issues in a high profile, immediate environment is required. Ability to adapt and change as the needs of business dictates. Location Cootehill, County Cavan, Ireland Seniority level Mid‑Senior level Employment type Full‑time Job function Production and Manufacturing Industries Hospitals and Health Care #J-18808-Ljbffr
The Senior Quality Engineer will support and execute strategic initiatives across the full spectrum of quality systems, including complaint handling, CAPA, audit readiness, document control, and regulatory compliance. Main Responsibilities Coordinate cross‑functional efforts across Quality, IT, and other business units to implement and maintain robust quality system processes. Ensure compliance with ISO 13485, 21 CFR 820 Quality System Regulations, and other applicable regulations by providing guidance, performing gap analyses, and leading improvement activities. Support the development, enhancement, and maintenance of enterprise‑wide quality applications such as complaint handling, CAPA, audit management, and document control. Manage project scope, timelines, risks, and resources to ensure successful execution of quality‑related initiatives. Analyze business needs and translate them into actionable project plans, system requirements, and process improvements. Conduct stakeholder reviews to prioritize system enhancements and ensure alignment with business and regulatory objectives. Monitor project performance and communicate progress through reports and dashboards to stakeholders and leadership. Apply risk assessment and problem‑solving techniques to resolve complex quality and system issues. Support internal and external audits, perform gap analyses, and lead implementation of compliance improvements. Investigate and resolve quality system nonconformances identified during audits. Analyze audit findings and recommend modifications to products or standards; proactively identify opportunities for system compliance improvement. Promote a culture of continuous improvement and regulatory excellence across all quality system domains. Knowledge, Skills & Experience Bachelor’s degree in engineering, Life Sciences, or a related field. 5+ years of experience in Quality Assurance and Project Management within a regulated industry. Strong knowledge of ISO 13485, 21 CFR 820, and global quality systems. Proven experience managing cross‑functional projects and delivering results. Excellent analytical, problem‑solving, and decision‑making skills. Preferred Experience with enterprise quality systems (e.g., Salesforce, TrackWise, Agile). PMP or Six Sigma certification. Familiarity with enterprise platforms and system implementation. Strong communication and stakeholder engagement skills. Location Galway, County Galway, Ireland Seniority Level Mid‑Senior level Employment Type Full‑time Job Function Quality Assurance Industries Hospitals and Health Care #J-18808-Ljbffr
A leading healthcare company is seeking a Senior Quality Engineer based in Galway, Ireland. This role involves coordinating quality system processes, ensuring compliance with regulatory standards, and managing cross-functional projects. The ideal candidate will hold a Bachelor’s degree in engineering or Life Sciences and possess over 5 years of experience in Quality Assurance. This is a full-time position with a focus on quality improvement and project management. #J-18808-Ljbffr
A global healthcare leader is seeking a Design Assurance Engineer for a full-time position in Galway, Ireland. The role involves implementing best-practice design controls, supporting product development, and ensuring compliance with regulatory standards. Candidates should have a degree in Science, Engineering, or Technology, along with 2–3 years of relevant experience in a regulated environment. Excellent communication skills and the ability to work in diverse teams are essential. #J-18808-Ljbffr
Operational Excellence & Lean Specialist 3 days ago Be among the first 25 applicants 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 114,000 colleagues serve people in more than 160 countries. Abbott has been operating in Ireland since 1946 and serves the Irish market with a diverse range of healthcare products including diagnostics, diabetes care, medical devices and nutritional products. In Ireland, Abbott currently employs about 6,000 people across ten sites located in Dublin, Donegal, Clonmel, Cootehill, Galway, Kilkenny, Longford and Sligo. Abbott Diabetes Care has opened a new site in Kilkenny, at the forefront of diabetes care with the latest technology, to manufacture FreeStyle blood glucose test strips and FreeStyle Sensors for use in diabetes management. Among Abbott Diabetes Care leading brands are the FreeStyle Precision, FreeStyle Lite and FreeStyle Libre systems. Main Purpose of the role In this role you will be part of the Business Excellence team. As an Operational Excellence & Lean Specialist, you will play a key role in driving continuous improvement initiatives across the Kilkenny site. This role is ideal for a results‑driven professional with a passion for Lean methodologies, cross‑functional collaboration, and delivering measurable business impact. Main Responsibilities Lead and support Lean and continuous improvement initiatives across the site. Facilitate workshops and Kaizen events to identify and implement process improvements. Collaborate with cross‑functional teams to deliver high‑impact projects aligned with strategic goals. Apply Lean Six Sigma tools and methodologies to drive efficiency and eliminate waste. Track and report on project outcomes, ensuring delivery of tangible business benefits. Support the development and deployment of standard work and best practices. Promote a culture of continuous improvement through coaching and training. Qualifications And Experience Bachelor’s degree in engineering, Business, or related field. Lean Six Sigma Green Belt certification required; Black Belt desirable. Proven experience in leading or supporting cross‑functional project teams. Demonstrated success in project delivery with measurable benefits. Strong analytical, facilitation, and communication skills. Experience in a regulated manufacturing or healthcare environment is a plus. What We Offer Attractive compensation package that includes competitive pay, as well as benefits such as Family health insurance Excellent pension scheme Life assurance Career Development Fantastic new facility Growing business plus access to many more benefits Connect with us at www.abbott.com or https://www.ie.abbott/, on LinkedIn at www.linkedin.com/company/abbott-/, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews. Abbott is an equal opportunities employer. Seniority level Mid‑Senior level Employment type Full‑time Job function Production and Manufacturing Industries Hospitals and Health Care County Laois, Ireland €30,000.00-€32,000.00 2 weeks ago Clonmel, County Tipperary, Ireland 3 weeks ago Carlow, County Carlow, Ireland 2 weeks ago #J-18808-Ljbffr
A global healthcare leader is seeking a professional to ensure software quality and compliance in Kilkenny. You will lead validation activities, develop documentation, and perform compliance assessments in a dynamic environment. Ideal candidates have a degree in IT, Engineering, or Science, and 4-5 years of relevant experience. Join us to set the standard for software quality excellence in healthcare technology. #J-18808-Ljbffr
Join to apply for the Design Assurance Engineer - IVDR role at Abbott . About Abbott Abbott is a global healthcare leader, committed to helping people live their best possible life through the power of health. For more than 135 years, we have brought new products and technologies to the world in diagnostics, nutrition, cardiovascular, medical devices, and branded generic pharmaceuticals – creating more possibilities for people at all stages of life. Today our 115,000 Abbott colleagues are working to help people live not just longer, but better, in the more than 160 countries we serve. Job Location Galway, County Galway, Ireland Description The global Design Assurance team for IDEM, the Infectious Diseases Emerging Market Business Unit, supports R&D, Marketing, Clinical Operations, RA, QA, and manufacturing functions across Europe, Asia, and the US. The team is responsible for Design Control throughout the lifecycle of NPI projects, from ideation through to product launch including sustainment, for the realization of our Lateral Flow Diagnostic Devices. The team supports a rapidly expanding business unit within Abbott. To ensure we can rapidly expand our Design Assurance capability, we are recruiting a Design Assurance Engineer who will strengthen the team through the implementation of best‑practice design controls within our projects. The Design Assurance Engineer role will be instrumental in shaping the NPI Project deliverables to support our IDEM new product development pipeline. They will provide direction and ensure compliance across all our core and extended teams – R&D, Marketing, QA, RA, Clinical Operations, and Manufacturing. Please note this position is a 12‑month FTC. Responsibilities And Duties Promote awareness of regulatory and customer requirements throughout the organization. Remediate current Design Control procedures and practices across sites to standardize to “best‑in‑class” design controls. Liaise with quality systems and regulatory affairs personnel to ensure compliance and drive alignment and harmonization. Deploy effective training collateral to ensure compliance with design control policies with the core teams, extended teams, and relevant functions within the business unit. Embed Design Assurance in all stages of design concept and feasibility to support R&D through specification setting, test development, and provision of statistical sampling to ensure robust prototypes and design at design freeze. Support new test development and appropriate test method validation. Provide ongoing risk management, design control, quality systems, and overall design assurance expertise and leadership to the project core and extended teams. Perform technical reviews of design documentation and labeling, attend design reviews, coordinate and facilitate completion and update of design risk management documentation, and act as independent reviewer for all design activities including design changes. Escalate design control concerns/ issues in a timely manner to ensure project schedule maintenance. Support design control for audits including Abbott corporate audits and external regulatory/governing body audits (e.g., FDA/WHO). Work in a matrix organization where project deliverables are accountable to the program/workstream leader. Requirements Primary degree-level qualification in Science, Engineering or Technology, plus 2–3 years of quality engineering/design assurance work experience within a regulated environment (ISO 13485/FDA). Formal training in medical device risk management, process validation, software validation, and problem solving would be beneficial. Excellent data analytics skills. Proven ability to work well as part of a team and independently. Excellent communication skills to support virtual project requirements. Clear demonstrated experience working in a diverse cultural environment. Excellent presentation skills to facilitate communication throughout the organization. In addition, excellent use of virtual communication technology is required for effective workshop leadership and change management. Travel pending company policy, global and country regulations to Asia and Europe. Seniority level Entry level Employment type Full‑time Job function Quality Assurance Industries Hospitals and Health Care #J-18808-Ljbffr
A global healthcare leader is seeking a Materials Planner for their Cootehill, Ireland facility. This mid-senior level role involves coordinating supply chain processes to align output with market needs. Candidates should have relevant experience in manufacturing and a degree in purchasing or production planning. Excellent communication, teamwork, and analytical skills are essential. The position is full-time, offering an opportunity in a fast-paced environment. #J-18808-Ljbffr
