9 Abbott jobs in Ireland

Manufacturing Engineer Waterford, County Waterford, Ireland Are you an engineer with a passion for building, problem-solving, and driving continuous improvement? This is an exciting opportunity to join a leading medical device manufacturer where you'll play a pivotal role in shaping processes that deliver safety, quality, and productivity. The Role As a key member of the engineering team, you will: Lead Engineering Change Notices (ECNs) and ensure smooth, timely implementation. Manage validation activities and oversee First Article Inspection (FAIR) reporting. Support New Product Introductions (NPI), acting as a project lead and working closely with customers and cross-functional teams. Provide CAD support, prepare technical drawings, and design jigs and fixtures. Define and optimise manufacturing and assembly processes, including external subcontract processes. Ensure compliance with SOPs and production system requirements. Drive continuous improvement initiatives to reduce waste and enhance efficiency. Stay current with new technologies and best practices within manufacturing. What We're Looking For Bachelor's degree in Engineering. 3-5 years' experience in medical devices or another highly regulated industry (pharma, aerospace, automotive). CAD experience (SolidWorks or equivalent). Familiarity with investigative techniques and statistical analysis tools (e.g., Minitab) desirable. Strong problem-solving mindset and a passion for process improvement. Why Join? You'll be part of a forward-thinking company at the forefront of advanced manufacturing, working on innovative projects that directly impact patient outcomes. This role offers excellent scope for career development, exposure to cutting-edge technologies, and the chance to make a real difference in a regulated, high-quality environment. Skills: Manufacturing Medical Devices Process

Project Manager Galway Job Title: Project Manager Location: Galway, Ireland Industry: Medical Device Manufacturing About the Company We are now hiring for a Project Manager for a leading medical device manufacturing company based in Galway, committed to delivering innovative and life-enhancing solutions in healthcare. We are currently seeking an experienced Project Manager to join our dynamic team and play a pivotal role in the successful execution of cross-functional projects. About the role: As a Project Manager, you will lead cross-functional teams in the planning, execution, and delivery of complex and CAPEX projects within our manufacturing operations. You will be responsible for managing the full project lifecycle, from initial scoping through to execution and close-out, with a focus on equipment introduction, process improvements, and supplier/vendor coordination. Responsibilities: Project Leadership: Lead the planning, coordination, and execution of manufacturing and engineering projects, ensuring alignment with strategic goals. Scoping & Planning: Define project scope, objectives, deliverables, and timelines in collaboration with stakeholders. Cross-functional Collaboration: Work closely with internal departments (R&D, Quality, Manufacturing, Regulatory, and Supply Chain) to drive project success. Equipment Introduction: Manage the introduction and qualification of new manufacturing equipment and technologies, including FAT, SAT, IQ/OQ/PQ processes. Stakeholder Management: Interface with internal and external stakeholders to ensure alignment, clear communication, and timely updates on project progress. Supplier & Vendor Management: Source, evaluate, and manage relationships with suppliers and vendors to ensure timely delivery of project-related equipment and materials. Risk Management: Identify project risks and develop mitigation plans to ensure on-time and within-budget delivery. Reporting: Provide regular project updates, KPIs, and dashboards to senior management. Compliance: Ensure all activities adhere to company policies, industry standards, and applicable regulatory requirements (e.g., ISO 13485, FDA, MDR) Requirements: Bachelors degree in Engineering, Science, or a related technical field. Minimum of 5 years of experience in project management within a regulated manufacturing environment, preferably medical devices. Proven experience managing cross-functional projects including equipment introduction and supplier/vendor coordination. Strong understanding of GMP, ISO 13485, and FDA requirements. Project Management certification (e.g., PMP, PRINCE2) is an advantage. Experience with project management tools (e.g., MS Project, Smartsheet, JIRA). Excellent leadership, communication, and problem-solving skills. Ability to manage multiple priorities and work under pressure in a fast-paced environment. For more information on this opportunity please reach out or send your CV to Contact: Gary Keane - INDCRG Skills: People management project planning manufacturing GMP scoping budgeting PMP

New Product Introduction Engineer (Med Device) No NPI experience needed. Open to Engineers with manufacturing experience, stakeholder experience and project experience. Our client is at the forefront of medical device innovation, and they're looking for an NPI Engineer to join their dedicated team, reporting to the Lead NPI Engineer. This role is crucial for executing and delivering strategic projects that enhance manufacturing capacity and capability. You'll be involved in every stage of project delivery, from initial feasibility studies through to manufacturing start-up and seamless handover to the operations team. Key Responsibilities: Develop and refine manufacturing processes for new medical device projects. Manage multiple small to medium-scale projects, guiding them from concept through design for manufacture, commissioning, and qualification. Generate project proposals, plans, scopes of work, cost estimates, and quotations. Control the transfer of new product manufacturing processes to production. Liaise effectively with customer representatives, managing expectations regarding project progress, scope, and budget. Coordinate with various internal functional groups including EHS, QA, Manufacturing, Engineering, Supply Chain, Facilities/Maintenance, and Validation to ensure comprehensive project delivery. Track and report on project costs, schedules, targets, and achievements directly. Review and approve documentation, including specifications and drawings, and generate work instructions and action change notes. Manage internal and external teams to meet project schedules. Provide qualification and troubleshooting support for equipment and processes. Independently manage technical, engineering, and compliance matters, making decisions on engineering problems and methods. What We're Looking For 2-5 years of relevant experience in project management or research & development, ideally within a medical devices environment. We will also consider candidates from other similar regulated industries such as pharmaceuticals. A Bachelor's Degree (Honors) in Engineering (Level 8). Manufacturing exp with strong stakeholder experience and project experieince. Ideally, you'll also have: Proficiency in a CAD package such as SolidWorks, or equivalent. Working experience in a manufacturing environment that is ISO 13485 certified. Proficiency in an MRP package such as SAP. Work Environment This role operates within a normal manufacturing environment. The successful candidate will be expected to adhere to all safety regulations, maintain a clean and orderly work area, and wear appropriate Personal Protective Equipment (PPE) as required. Flexibility to support company needs is essential. If you're an experienced and proactive NPI Engineer looking to make a significant impact within a leading medical devices company, we encourage you to apply. Skills: NPI Process Manufacturing

**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 in Ireland**
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 Kilkenny**
Abbott Diabetes Care has opened a new site, in Kilkenny, that is 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.
**This is how you can make a difference at Abbott:**
As a Lead Operator, in Abbott, Kilkenny you will ensure that production targets and schedules are achieved for their line.
Assist the Operations team lead in achieving the goals of the process area.
Provides guidance and a source of information for operators and support groups in the area.
Responsible for their line's performance with respect to safety, quality, on-time delivery and cost
**Your main responsibilities will be:**
+ Co-ordinates aspects of the production area workflow (i.e. people, products, and materials) to meet Master Schedule requirements.
+ Coordinates work assignments within the production department that includes training, technical support and/or process/trouble shooting support.
+ Works with internal resources to resolve problems.
+ As the Process Line Subject Matter Expert (SME), represents production on projects when needed and train other employees when necessary.
+ Responsible for the startup and shut down of their line or area.
+ Coordinate break schedules and assist with machine operation during breaks.
+ Assembles, repairs, inspects and/or tests products following written instructions. Ability to read and comprehend basic instructions and other work-related documents, written in English.
+ Set up and operates a variety of manufacturing machines or equipment following written instructions in the English language.
+ Clean tools and equipment per documented procedures.
+ Record information on approved documents.
+ Responsible for compliance with applicable corporate and divisional policies and procedures.
+ Solves a wide range of complex problems requiring advanced interpretation of generally defined procedures and practices.
**QUALIFICATIONS AND EXPERIENCE**
+ Minimum education - Leaving Certificate.
+ Previous experience in manufacturing operations, preferably in a Senior Operator role, with demonstrated ability to acquire and apply manufacturing principals is preferred.
+ Experience working in a highly automated, high volume manufacturing environment preferred. Previous experience working in the medical device, pharma, automotive, tech, food industries preferred.
+ Ability to work effectively within a team in a fast-paced changing environment. Multi-tasks, prioritizes and meets deadlines in timely manner. Strong organizational, planning, and follow-up skills and ability to hold others accountable.
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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

SSA are recruiting a LOTO Engineer for an on-site, local-hire role in Ireland, focused on Lockout/Tagout within the MedTech industry. This position is urgent and exclusive to candidates based in Ireland. Key Details Position: LOTO (Lockout/Tagout) Engineer Industry: Medical Devices / Safety Engineering / Compliance Location: Ireland (On-site; local candidates only) Type: Full-Time, Permanent Salary:€60,000 - €70,000& Package Full Job Description Our client is a respected MedTech manufacturer with operations across Ireland. They are now seeking a skilled LOTO Engineer to lead hazardous-energy control during equipment maintenance. This permanent, on-site position will be central to safeguarding staff, patients, equipment integrity, and regulatory compliance. Key Responsibilities Identify and document all energy sources (electrical, mechanical, pneumatic, hydraulic, etc.) Develop and implement detailed Lockout/Tagout procedures for medical and service equipment Deliver training for staff on LOTO protocols; conduct audits to verify adherence Oversee LOTO implementation during maintenance and servicing operations Maintain accurate records of LOTO activities, training sessions, and audits Ensure practices align with OSHA and EU safety and regulatory standards Investigate LOTO-related incidents or near-misses; drive corrective actions Qualifications & Experience Bachelors degree or diploma in Engineering, EHS, or related field 36 years experience managing LOTO programmes in MedTech or manufacturing Strong understanding of hazardous energy control best practice and standards Experience collaborating with maintenance teams and completing safety audits Excellent communication, documentation, and stakeholder engagement skills How to Apply Please reach out to Conor ODonnell at SSA Group for a confidential conversation at or Skills: EHS LOTO Engineering LOTO Safety Environmental Health & Safety Safety Medical Devices

Location: Galway (On-site)
Industry: Medical Device / Start-up
Our client, a dynamic and fast-paced medical device start-up based in Galway, is seeking a Quality Engineer I to join their growing team. The company is focused on developing innovative, patient-centric technologies to improve quality of life and is advancing rapidly through the product development lifecycle toward global market launch.

This role offers a unique opportunity for a motivated and hands-on quality professional to apply their engineering knowledge across multiple areas of a developing Quality Management System. The ideal candidate will enjoy working in a cross-functional, start-up environment and contributing directly to impactful product development.

Responsibilities include but are not limited to the following:

• Apply quality engineering expertise across the Quality Management System (QMS).

• Support certification and maintenance of compliance to ISO 13485 and 21 CFR Part 820.

• Assist with design assurance activities, including design controls, verification, and validation.

• Support development and validation of test methods and computer system assurance programs.

• Participate in risk management and usability engineering activities.

• Maintain document control through QT9 eQMS and perform related administrative tasks.

• Contribute to the CAPA and non-conformance (NC) investigation and resolution process.

• Assist in internal and external audits and implement corrective actions as needed.

• Support updates and gap assessments for applicable regulatory standards and guidance.

• Participate in supplier quality management, vendor evaluation, and AVL maintenance.

• Collaborate cross-functionally to uphold quality objectives and continuous improvement.

• Perform additional quality-related duties to support business goals and KPIs.

• Bachelor’s degree in engineering, science, or related field (or equivalent).

• Minimum of 2 years' experience in a medical device or supplier environment.

• Familiarity with ISO 13485, FDA QSR (21 CFR Part 820), and GMP requirements.

• Experience in both FDA and European regulatory environments is preferred.

• Strong initiative, problem-solving, and follow-through in executing responsibilities.

• Understanding of risk management methodologies (ISO 14971).

• Experience with sterilization (EtO/Gamma), biocompatibility, and transportation testing is a plus.

• Prior involvement in audits or inspections is an advantage.

• Proficiency in MS Office and familiarity with electronic QMS tools.

Immediate interviews available for suitable candidates.

Note: By applying for this position, you may also be considered by Pale Blue Dot® Recruitment for other future vacancies

 Pale Blue Dot® Recruitment

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**FIXED TERM CONTRACT**
**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 Nutrition**
Our nutrition business develops science-based nutrition products for people of all ages, from helping babies and children grow, to keeping adult bodies strong and active. Millions of people around the world count on our leading brands - including Similac®, PediaSure®, Pedialyte®, Ensure®, Glucerna® and ZonePerfect® - to help get the nutrients they need to live their healthiest life.
**PURPOSE OF THE JOB**
As a Medical Safety & Surveillance (MSS) Global Medical Device Manager, the candidate will use his/her in-depth understanding of medical devices to ensure compliance with regulatory requirements for Abbott Nutrition medical devices. The MSS Global Medical Device Manager will have responsibility for generating documentation that supports Abbott Nutrition's global medical device registration and on-going compliance with EUMDR. This may include development and implementation of global standardized operating procedures. The candidate may also lead the development/maintenance of local medical device vigilance systems (predominantly for UK and EU), ensuring compliance with local regulations. The candidate will have departmental, cross functional, and global influence, and will be considered a medical device subject matter expert within the company.
**MAJOR RESPONSIBILITIES**
+ Organizes, manages and maintains a highly compliant global medical device system for Abbott Nutrition.
+ Maintains awareness and ensures compliance with established and updated local and global medical device processes as well as local and global regulations and guidelines for medical device registration and post-market documentation.
+ Develops and implements training programs for individuals involved in medical device activities.
+ Monitors medical device system performance; tracks compliance metrics and reports to global MSS Leadership Team.
+ Ensures global/local medical device audit readiness; Supports medical device audits/inspections and leads activities related to corrective and preventative actions for any audit findings.
+ Actively contributes to activities related to the monitoring of safety profiles for Abbott Nutrition products registered as medical devices, such as signal detection, evaluation, and prioritization.
+ Reviews and provides input to product DFMEAs.
+ Assists local staff with drafting and implementation of Safety Data Exchange Agreements, if applicable.
+ Works cross-functionally with Regulatory Affairs and Quality Assurance functions to maintain current knowledge of regulatory safety reporting guidelines and implementing relevant guidelines into practices and procedures.
+ Assists in the preparation, review and submission of aggregate safety reports.
+ Accountable for strategic preparation of medical device regulatory submission documentation (i.e. CEP, CER, PSUR, PMCF etc) and on-time completion of these activities for the division.
**EDUCATION & COMPETENCIES**
+ Master's degree in related health science or equivalent skills, education, or experience.
+ RAC certification is a plus.
+ 5-7 years of experience and proficiency in medical device regulatory submissions to Notified Bodies under EUMDR / MedDEV and knowledge of Medical Device standards and guidelines (such as ISO, GSPR, and MDGC).
+ Solid understanding and working knowledge of medical device regulatory requirements and in the development and implementation of processes to maintain compliance.
+ Strong medical knowledge and understanding to support safety related activities; background/experience with nutrition/nutritional products is a plus.
+ Knowledge of Vigilance reporting regulations on a Global scale.
+ Minimum 3 years of experience in leading complex projects or programs; global/regional experience desirable.
+ Fluency in spoken/written English;
+ Computer proficient (Windows, Word, Excel); experience working in adverse event databases.
+ Excellent communication and interpersonal skills, both written and spoken.
+ Strong organizational skills with proven ability to prioritize and work on multiple tasks and projects.
+ Strong commitment to compliance with the relevant rules and procedures and to scientific quality and integrity.
+ High level of accountability and reliability.
+ Demonstrates ability to work productively as a team.
+ Ability to work in a fast paced, changing environment.
+ Ease of operating in high stress, big decision situations.
+ Continuous improvement mindset.
+ Ability to influence a team in a positive way in relation to performance, change, and culture.
+ Demonstrate broad knowledge of Abbott's business and how department processes/responsibilities interconnect.
+ Mastery of the inventory deployment planning process.
+ Exceptional problem-solving skills
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

Location: County Tipperary (On-site)
Contract: 12-Month Fixed Term (with potential for extension)

Our client, a well-established engineering firm, is seeking a Tooling & Equipment Design Engineer to support the development of custom tooling and mechanical systems for implantable medical devices. The role is based on-site at a world-class manufacturing facility in County Tipperary. This is a hands-on, technically challenging role ideal for an experienced mechanical engineer who enjoys precision design, collaboration, and seeing their work make a real-world impact.

Responsibilities include but are not limited to:

• Design and develop mechanical tooling, fixtures, and assembly equipment to support advanced medical device manufacturing.

• Create detailed 3D models and engineering drawings using CAD (preferably SolidWorks).

• Collaborate with manufacturing, quality, and product development teams to ensure seamless integration of new equipment and processes.

• Participate in design reviews, technical problem-solving, and continuous improvement initiatives.

• Liaise with external vendors, suppliers, and equipment manufacturers to ensure quality and timely delivery of components.

• Support the validation and qualification of new equipment and processes as required.

• 3+ years of mechanical design experience, ideally in tooling, fixtures, or automation within a medical device or regulated manufacturing environment.

• Strong proficiency in CAD (SolidWorks preferred).

• Solid understanding of mechanical engineering principles, materials, and production techniques.

• Proven ability to deliver detailed and accurate mechanical designs within project timelines.

• Excellent problem-solving skills and attention to detail.

• Strong communication and teamwork skills.

Note: By applying for this position, you may also be considered by Pale Blue Dot® Recruitment for other or future related vacancies.

 Pale Blue Dot® Recruitment

The Experts in STEM Workforce Solutions