39 Merck jobs in Ireland

Job Title: Quality Assurance Manager Location: Drogheda, Ireland Salary: €45,000 DOE Overview: An excellent opportunity has arisen for an experienced Quality Assurance Manager to join a leading FMCG food manufacturer with a portfolio of well-known household brands. This is a fantastic chance to become part of a business with ambitious growth plans, where you will play a key role in maintaining the highest standards of food safety and quality. Key Responsibilities: Lead and continuously improve the FSSC22000 certified quality management system. Act as the site champion for quality, ensuring standards are consistently met and exceeded. Manage and oversee internal auditing to ISO/FSSC standards. Lead the HACCP team and take ownership of allergen management. Manage incoming inspections and carry out daily quality control checks. Oversee hygiene and food safety auditing across the site. Partner with New Product Development to ensure quality standards in innovation projects. Deliver staff training on QA procedures and hygiene practices. Maintain sampling plans and coordinate laboratory analysis of raw materials. Manage raw material supplier approval, specifications, and documentation for both raw materials and finished goods. Liaise with Customer Services on complaint investigations, ensuring timely resolutions. Act as the technical point of contact for regulatory bodies and customers. Contribute as a member of the site Health & Safety Team. Present updates and insights at weekly stand-up meetings. The Person: 4-5 years' experience in a Quality role within FMCG food manufacturing. Strong knowledge of Food Safety and Quality Management Systems (FSSC22000 & BRC). Proven ability to work independently as well as collaboratively in a team. A continuous improvement mindset with strong attention to detail. Demonstrated leadership skills with the ability to influence and engage teams. Excellent communication and IT skills. Skills: QA Quality Assurance

Catalyx is seeking a Quality Assurance Specialist to join our team and work on our customer site in Cork. This role operates on a rotating weekly shift pattern, alternating between morning and evening shifts. Who We Are: Catalyx specializes in the science of operational processes. With a footprint across North America and Europe, the company carefully automates and services R&D, production, packaging, and delivery processes-globally-with a sophisticated blend of products, technologies, and lifecycle services. The company was formed in 2022 after CXV Global (Crest Solutions, Xyntek, and VistaLink) and Panacea Technologies joined forces. For over three decades, Catalyx's partnership-based culture has helped organizations in production-intense, highly regulated industries optimize their operational efficiency, performance, and safety. To learn more about the company's experience and comprehensive suite of capabilities and solutions, visit . The Role: Catalyx is a trusted partner in delivering world-class lifecycle services to regulated and high-risk end markets. With a relentless commitment to innovation and excellence, we partner with life science and other highly regulated organisations, to empower them to enhance efficiency, and drive success. As part of this commitment, we are continuously developing our on-site teams to support the advancement of customer operations. Responsibilities: Provide quality oversight across various production stages, including material inspection, in-process control, and product readiness activities. Assemble and review documentation to support product disposition, working closely with operational and quality colleagues to meet release timelines. Support packaging operations by conducting visual inspections and ensuring process adherence during routine activities. Collaborate with cross-functional teams (Manufacturing, Quality Control, Supply Chain, Engineering, etc.) to resolve day-to-day queries and issues efficiently. Contribute to the maintenance and improvement of quality systems through change control, deviation management, and CAPA oversight. Conduct documentation reviews such as batch records, SOPs, and WI updates, ensuring alignment with regulatory and internal standards. Participate in the preparation of periodic quality reports and metrics, supporting trend identification and ongoing improvement. Engage in internal audits and readiness assessments to ensure site and process compliance. Provide knowledge-sharing and informal coaching on quality processes to enable operational teams to work effectively within GMP frameworks. Support project-based work and initiatives aimed at process enhancement and improved compliance practices. Review and approve manufacturing inputs and documents to ensure compliance with release criteria. Requirements: Bachelor's degree in a scientific or technical discipline. Minimum 3 years' experience in a Quality or GMP-related role within the pharmaceutical, biotech or related regulated sector. Familiarity with batch documentation, quality systems, and regulatory expectations (e.g., FDA, EMA). Ability to analyse issues, identify appropriate corrective actions, and escalate where necessary. Experience supporting or interacting with packaging or material management processes is beneficial. Strong written and verbal communication skills; confident working in a collaborative environment. Competence with Microsoft Office tools, particularly Excel and Word. Organised, detail-focused, and capable of managing multiple priorities. Comfortable working independently within defined parameters, and adaptable to shifting project needs Why Join Catalyx? At Catalyx we understand that our people are our greatest asset. For this reason and many others, we take care of them. The team in Catalyx benefits from a Total Rewards package. This includes great personal benefits and professional growth opportunities. Catalyx is an Equal Opportunity Employer. We are committed to creating a diverse and inclusive workplace where all individuals are valued, respected, and supported. We do not discriminate on the basis of race, colour, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, disability, veteran status, genetic information, or any other characteristic protected by applicable law. We encourage applications from all qualified candidates, regardless of background, and strive to create a welcoming environment for everyone. At Catalyx, we are committed to attracting the best global talent. We proudly support our international employees by offering assistance with Critical Skills Visa applications for eligible candidates. To be considered for this role you will be redirected to and must complete the application process on our careers page. To start the process, click the Apply button below to Login/Register.

Build the future of financial markets. Build yours. Ready to make a real impact in the financial industry? At Deutsche Brse Group, we'll empower you to grow your career in a supportive and inclusive environment. With our unique business model, driven by 15,000 colleagues around the globe, we actively shape the future of financial markets. Join our One Global Team! Who we are Deutsche Brse Group is one of the world's leading exchange organisations and an innovative market infrastructure provider. With our products and services, we ensure that capital markets are fair, transparent, reliable, and stable. Together, we develop state-of-the-art IT solutions and offer our IT systems all over the world. Within the Deutsche Brse Group, Clearstream is an international central securities depository (ICSD). It provides post-trade infrastructure and securities services for the international market and 59 domestic markets worldwide, with customers in 110 countries. Cork Your career at Deutsche Brse Group Your area of work The Quality Control Officer is responsible for ensuring the accuracy, consistency, and completeness of regulatory reporting outputs across KIIDs, PRIIPs and ESG domains. This role supports the delivery of high-quality reports by performing detailed quality checks, identifying discrepancies, and driving continuous improvement in data validation and reporting processes. Your responsibilities Perform detailed quality control checks on KIIDs, PRIIPs and ESG reports prior to client delivery, ensuring alignment with regulatory standards and internal quality benchmarks. Identify and document errors, inconsistencies, and missing narratives across reporting outputs. Collaborate with Regulatory Reporting Agents to validate data sources and ensure accurate interpretation of regulatory requirements. Monitor and report on recurring quality issues, contributing to root cause analysis and recommending corrective actions. Support the enhancement of validation tools and processes to reduce false positives and improve reporting accuracy. Maintain quality logs and KPIs to track performance and support post-production reviews. Liaise with internal teams to ensure timely resolution of quality issues and escalate critical findings to management. Assist in the development and implementation of quality assurance procedures and best practices. Participate in assigned training and stay updated on regulatory changes impacting reporting standards. Act and work in compliance with all internal rules and policies. Your profile A minimum of 3 years of post-graduate education, preferably in Finance, Data Management, or a related field At least 2 years of experience in a quality assurance, data validation, or regulatory reporting role Understanding of ESG, KIID, and PRIIPs reporting standards and regulatory frameworks Proficiency in English; additional languages are an asset Advanced Microsoft Excel skills and familiarity with data validation tools Excellent attention to detail and analytical skills Strong communication and interpersonal skills Proactive, solution-oriented mindset with a collaborative approach Ability to work independently and manage multiple priorities

Job title:Quality Assurance Associate Location:Bishopstown, Cork. Benefits:Excellent salary, 10% bonus, hybrid working, healthcare and pension. Company: My client, spun out from Munster Technological University (formerly Cork Institute of Technology) in 2015, develops innovative ENT (Ear, Nose, and Throat) medical devices that simplify surgical procedures by enabling treatments to be conducted safely outside the operating roomtypically with just topical anesthesia. Role: You will be responsible for assisting in the maintenance of the Quality Management System (QMS), assist with the management of internal processes and external vendors to ensure product quality. This involves managing supplier relationships, participating in audits, resolving quality issues, driving continuous improvement initiatives and collaborate with various teams to maintain quality across the supply chain. The person in this position must have a working knowledge of medical device regulatory requirements and standard practices in the medical device industry. Job Requirements: Maintaining the effectiveness of the QMS and making continuous improvements to it. Managing day-to-day QA activities including frequent interface with contract manufacturers, QA consultants and testing contractors as well as handling multiple projects related to product and compliance enhancements. Responsible for assisting in notified body audits and internal audits. Maintain and coordinate quality system schedules, including: Supplier and internal audits; management review and documentation updates. Support the wider team to ensure product manufacture and testing meets the requirements. Building and maintaining strong relationships with suppliers, monitoring their performance, and conducting audits to ensure compliance with quality standards. Investigating, analysing, and resolving any product quality problems, including root cause analysis and implementing corrective and preventive actions. Ensuring that incoming materials meet the required specifications and working with the engineering team to address any quality concerns. Maintain the day-to-day activities of Post Market Surveillance, including, but not limited to: coordinating investigations between complainants and contract manufacturing sites follow up on corrective actions, when required Support with Significant Changes and Notified Body interactions. Carry out other quality related duties as required, inclusive of updates to procedures, forms, processes and periodic reviews. Education Bachelors degree in engineering or science. Quality certification in ISO 13485 a must. A minimum of 4 years of experience in a medical device QA position(s) role within a medical device organisation. Thorough understanding and knowledge of ISO 13485 and ISO 14971, EU MDR and 21 CFR Part 820. Desirable to have lead auditor certification and/or Regulatory certifications. Proven track record with the ability to successfully manage projects to deadlines. Good Documentation Practice experience. Report & Technical Writing experience. Project Management experience. Strong ability to manage critical projects as part of an interdisciplinary team. Excellent problem solving and communication skills. Does this sound like your next career move? To apply and For more info forward your application to the link provided or contact me on OR Benefits: Healthcare + Annual Bonus + Pension

Quality Assurance Technician A well-established manufacturer is seeking a Quality Assurance Technician to join their team in Limerick. This is a hands-on role supporting both new and existing production lines in a fast-paced environment. This role would suit someone who has worked in a production environment, had some involvement in quality, and is now looking to take a step up into a full-time quality role. The Role: Reporting to the Quality Manager, the QA Technician will play a vital role in maintaining and improving product quality standards. You'll collaborate closely with production, engineering, and maintenance teams, ensuring compliance with internal processes and industry regulations. Key Responsibilities: Perform in-process and final inspections on products Carry out routine and non-routine quality checks Use measurement tools (e.g. calipers, micrometers, gauges) Identify, document, and support resolution of quality issues Assist in root cause analysis and corrective actions Review and maintain quality documentation in line with ISO standards Support audits and continuous improvement activities Oversee lab equipment calibration and QC analysis of raw materials Promote a clean, safe working environment in line with health & safety policy What You'll Need: Level 6 qualification in Quality Assurance (or related) 1-3 years' experience in a manufacturing or production setting Exposure to quality systems, procedures, and tools High attention to detail and problem-solving mindset Strong communication and teamwork skills Proficiency in Microsoft Office If you're ready to make the move into a dedicated quality role, this could be the ideal next step. To apply or learn more, contact Kerry on or send your CV today. Skills: Quality Assurance Benefits: Negotiable

Quality Assurance Technician Co Monaghan Fulltime/Permanent Monday - Friday, 40 Hours Attractive Salary Vickerstock are working in partnership with our specialist food processing client in Ireland and UK who have doubled production in the last 5 years and continues to do so, due to this they are seeking a full time/permanent Quality Assurance Technician to join the team at their site in County Monaghan. As a Quality Assurance Technician reporting to the Quality & Technical Manager, you will be responsible for: Lead the development, implementation, and monitoring of the Food Safety Management System (FSMS), including HACCP, prerequisite programmes, and SOPs. Ensure compliance with legislation, BRC, and customer standards, report performance and compliance status to the Technical Manager. Conduct and report internal audits, driving effective close-outs with management and supervisors. Investigate customer complaints and external non-conformances, ensuring robust root cause analysis and timely corrective/preventive actions. Analyse Production Quality KPIs, identify trends, and collaborate with production teams to resolve issues and drive improvement. Apply Lean principles in daily problem-solving, root cause analysis, and change management initiatives. Proactively identify hazards, manage risks, and implement continuous improvement measures to safeguard product safety. Lead and deliver cross-functional projects, ensuring timely completion and stakeholder engagement. Work closely with Production and Maintenance teams to set standards, solve problems, and implement sustainable solutions. We are looking for: Minimum recognised 3rd level qualification in a Food Science related discipline. Minimum 3 years+ Quality Assurance/Quality Control experience in Food Manufacturing environment Experience working with Quality Systems Have a demonstratable comprehensive knowledge of auditing, quality standards and systems, quality management techniques such as HACCP, Process Control, knowledge of food legislation, GFSI standards including BRC. Sound like the career move you've been after and would like to hear more, pick up the phone to Sophie now on or send an updated CV - in Word format - via the link on the page (or email). If this opportunity doesn't quite get the taste buds flowing but like me you are passionate about food, let's get a chat and see how I can help grow your career. PLEASE VISIT OUR WEBSITE FOR A FULL LIST OF OUR CURRENT VACANCIES. Skills: Quality Assurance Technician Quality Technician Quality Assurance Quality Control Senior Quality

Job Title: Quality Assurance Technician Reporting to: Quality & Technical Manager Contract Type: Full-time, Permanent Location: Co. Monaghan Salary: €45,000 - €50,000 (DOE) Overview We are seeking an experienced Quality Assurance Technician to join a leading food manufacturing business based in Co. Monaghan. This role offers the opportunity to play a key part in driving quality and compliance across the site, ensuring the highest standards in food safety and technical performance. Key Responsibilities Support the effective development, implementation, and monitoring of the Food Safety Management System, including HACCP, prerequisite programmes, and SOPs. Report on site performance against standards, ensuring compliance with legislation, BRC, and customer requirements. Conduct internal audits, communicate findings, and collaborate with management to ensure timely and effective close-outs. Lead and manage projects to completion, engaging key stakeholders throughout. Apply Lean manufacturing principles to problem-solving, root cause analysis, and change management. Proactively identify and mitigate product safety risks, implementing corrective and preventative actions to drive continuous improvement. Analyse production quality KPIs, report trends, and collaborate with production teams to resolve issues. Investigate customer complaints and non-conformances, ensuring robust root cause analysis and timely corrective actions. Work closely with Production and Maintenance teams to set standards, address issues, and implement improvements. Requirements Degree or equivalent qualification in Food Science or related discipline. Minimum of 3+ years' QA/QC experience within a food manufacturing environment. Strong knowledge of auditing, HACCP, food legislation, BRC, and quality systems. Proven experience in continuous improvement and delivering sustainable change. Strong analytical and problem-solving skills, with a proactive and hands-on approach. Highly motivated team player with excellent communication and interpersonal skills. Proficiency in Excel and other IT systems. Strong organisational and time management skills, with the ability to thrive in a fast-paced environment. Skills: QA Technician

Description
AWS Infrastructure Services is seeking an exceptional Quality Assurance Cabling Manager to lead a data center quality team in our Global Network Delivery organization. As a key leader in our infrastructure team, you will drive best-in-class cabling quality across AWS' global data centers, helping us maintain our position as the world's most efficient and cost-effective cloud infrastructure provider.
In this role, you will lead a team of Quality Assurance (QA) Engineers, establishing and maintaining the highest quality standards for our data center network deployments. Your team will be instrumental in ensuring that all build, scaling, and hardware installations meet AWS's rigorous quality guidelines, ultimately enabling seamless cloud services for our customers worldwide.
AWS Infrastructure Services owns the design, planning, delivery, and operation of all AWS global infrastructure. In other words, we're the people who keep the cloud running. We support all AWS data centers and all of the servers, storage, networking, power, and cooling equipment that ensure our customers have continual access to the innovation they rely on. We work on the most challenging problems, with thousands of variables impacting the supply chain - and we're looking for talented people who want to help.
You'll join a diverse team of software, hardware, and network engineers, supply chain specialists, security experts, operations managers, and other vital roles. You'll collaborate with people across AWS to help us deliver the highest standards for safety and security while providing seemingly infinite capacity at the lowest possible cost for our customers. And you'll experience an inclusive culture that welcomes bold ideas and empowers you to own them to completion.
#DCPD_GND
Key job responsibilities
- Lead and develop a diverse team of Quality Assurance Engineers and Data Center Auditors
- Establish and oversee comprehensive quality control systems, including inspection mechanisms and performance measurements
- Partner with network design teams and vendors to develop and enforce installation standards
- Manage end-to-end quality metrics, risk management, and preventative measures
- Drive continuous improvement through data-driven process optimization
- Conduct regular site audits and develop remediation strategies
- Serve as the primary quality assurance subject matter expert for cabling and hardware installations
- This position requires 25% travel within the region to AWS Data Centers for project reviews and onsite coordination.
A day in the life
Your typical day will involve collaborating across multiple disciplines and time zones. You'll start by reviewing quality metrics from previous days inspections and audits and addressing any immediate concerns with your team. Throughout the day, you'll conduct one-on-one meetings with team members, participate in cross-functional planning sessions, and analyze trend data to identify improvement opportunities.
You'll work directly with QA Engineers and managers to refine structured cabling and installation standards, and visiting data centers to ensure compliance and gather insights for continuous improvement. You will find yourself leading technical whiteboard sessions to resolve implementation challenges and presenting quality metrics to senior leadership.
About the team
As part of AWS Infrastructure, our organization prepares, plans, and builds the data centers that comprise the AWS cloud. This team drives continuous improvement of AWS Data Centers to provide more efficient and reliable infrastructure to customers.
Diverse Experiences
AWS values diverse experiences. Even if you do not meet all of the qualifications and skills listed in the job description, we encourage candidates to apply. If your career is just starting, hasn't followed a traditional path, or includes alternative experiences, don't let it stop you from applying.
Why AWS?
Amazon Web Services (AWS) is the world's most comprehensive and broadly adopted cloud platform. We pioneered cloud computing and never stopped innovating - that's why customers from the most successful startups to Global 500 companies trust our robust suite of products and services to power their businesses.
Inclusive Team Culture
Here at AWS, it's in our nature to learn and be curious. Our employee-led affinity groups foster a culture of inclusion that empower us to be proud of our differences. Ongoing events and learning experiences, including our Conversations on Race and Ethnicity (CORE) and AmazeCon conferences, inspire us to never stop embracing our uniqueness.
Mentorship & Career Growth
We're continuously raising our performance bar as we strive to become Earth's Best Employer. That's why you'll find endless knowledge-sharing, mentorship and other career-advancing resources here to help you develop into a better-rounded professional.
Work/Life Balance
We value work-life harmony. Achieving success at work should never come at the expense of sacrifices at home, which is why we strive for flexibility as part of our working culture. When we feel supported in the workplace and at home, there's nothing we can't achieve in the cloud.
Inclusive Team Culture
AWS values curiosity and connection. Our employee-led and company-sponsored affinity groups promote inclusion and empower our people to take pride in what makes us unique. Our inclusion events foster stronger, more collaborative teams. Our continual innovation is fueled by the bold ideas, fresh perspectives, and passionate voices our teams bring to everything we do.
Basic Qualifications
- Bachelor's degree or equivalent combination of education and experience
- 5+ years in management/team lead function
- 3+ years in a data center technology role or experience with network pathway infrastructure systems
- Demonstrated ability to lead and develop teams with excellent communication
- Strong analytical and problem-solving skills
Preferred Qualifications
- Familiarity with ISO9001, ISO11801, TIA568C, TIA942, and/or ANSI/BICSI
- Skilled at analyzing data and influencing executive decisions without direct authority
- 3+ years of knowledge in network cabling, optic types, and test equipment
- Experience with physical data center construction, particularly copper/fiber cabling, Quality assurance methodology and tools experience such as Six-Sigma certification or similar qualification
Amazon is an equal opportunities employer. We believe passionately that employing a diverse workforce is central to our success. We make recruiting decisions based on your experience and skills. We value your passion to discover, invent, simplify and build. Protecting your privacy and the security of your data is a longstanding top priority for Amazon. Please consult our Privacy Notice ( ) to know more about how we collect, use and transfer the personal data of our candidates.
Amazon is an equal opportunity employer and does not discriminate on the basis of protected veteran status, disability, or other legally protected status.
Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit for more information. If the country/region you're applying in isn't listed, please contact your Recruiting Partner.

**Abbott in Ireland**
Abbott serves the Irish market with a diverse range of healthcare products, including diagnostics, medical devices, and nutritional products. In Ireland, Abbott employs over 6,000 people across ten sites. 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**
Provide Process/Quality Engineering support to manufacturing and projects helping to ensure delivery of highest quality product to the customer. Provide Process/Quality Engineering support to product development teams, helping to ensure development of highest quality new products. Will be the liaison to cross function departments (for example Research and Development, Operations and other Quality Functions). Must be able to analyze data and assist in interpreting the data. Develop and implement investigation process improvements.
**MAJOR RESPONSIBILITIES**
+ Responsible for compliance with applicable corporate and divisional policies and procedures. Estimates project levels of effort and resource requirements by using standard estimating techniques and tools, and by working with appropriate staff to understand scope of effort.
+ Prepares project plans, schedules and budgets by using project management tools such as Microsoft Project and by working with appropriate staff to understand tasks necessary to complete project.
+ Directs project execution by assigning tasks, tracking project schedules, identifying risks, and developing and executing contingency plans.
+ Communicates project status by preparing standard status reports, and by participating in departmental and customer project status update meetings.
+ Resolves project issues by working with team members, project customers, and others as appropriate.
+ Translates business strategy into meaningful objectives and day-to-day activities required to accomplish them.
+ Identifies and controls manufacturing process defects (scrap, nonconforming material, customer complaints) by participating in efforts/teams focused on identifying the primary root causes and implementing corrective and preventative actions. May be responsible for querying and bounding data to support implementation of complex and documenting release criteria.
+ Develops product quality plans, documents and systems by creating product specifications, quality specifications and quality plans in conjunction with other product development team members. May be responsible for creating risk analyses and Failure Mode Effect Analysis (FMEA).
**EDUCATION & COMPETENCIES**
+ National Framework of Qualifications level 7 qualification in a relevant discipline and 4+years of related work experience, or an equivalent combination of education and work experience.
+ Wide application of technical principles, practices and procedures. Strong understanding of business unit function and cross group dependencies/relationships. Will perform this job in a quality system environment. Failure to adequately perform tasks can result in noncompliance with governmental regulations.
+ Works on problems of diverse scope where analysis of data requires evaluation of identifiable factors. Exercises judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions. Has a sound knowledge of various technical alternatives and their impact.
+ Establishes and cultivates an extensive network of support to facilitate completion of assignments. Participates in the development of less experienced staff by setting an example, providing guidance and work direction, and offering counsel. May lead a project team. Participates in determining goals and objectives for projects. Influences middle management on technical or business solutions. May interact with vendors.
+ Plans and organises non-routine tasks with approval. Initiates or maintains work schedule. Establishes priorities of work assignments. (Decision Making/Impact) Exercises judgment in selecting innovative, practical methods to achieve problem resolution. Failure to obtain results or erroneous decisions or recommendations would typically result in serious program delays and considerable expenditure of resources.
+ Works under only general direction. Independently determines and develops approach to solutions. Work is reviewed upon completion for adequacy in meeting objectives.
+ Will provide work direction and guidance to exempt and/or skilled nonexempt levels of employees will be asked to evaluate performance of and assist in career development planning for subordinates.
**REFER TO THE SITE SAFETY STAT** **E** **MENT (SHE ) FOR YOUR SA** **F** **ETY, HEALTH AND WELFARE AT WORK RESPONSIBILITIES**
**Abbott Ireland is an Equal Opportunities Employer**
Connect with us at , on LinkedIn at , on Facebook at and on Twitter @AbbottNews and @AbbottGlobal.
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email