473 Manufacturing jobs in Ireland

Requisition ID: 70680

Date: Sep 25, 2025

Location:
Dublin, Leinster, IE

Department: Engineering

Description:

At West, we're a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West's indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future?

There's no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families.

We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.

In this role, you will be responsible for developing new technology and supporting existing technology to improve production, quality, profitability and safety. This individual will be responsible for the planning, scheduling, execution of projects and communicating project status to targeted timelines. This individual will also manage/assist in facility expansion/modifications.

We have permanent and fixed term contracts available.

• Support development of new technology, existing technology and existing production lines to improve quality, profitability and safety.
• Develop, execute and document project assignments in compliance with committed timelines and project goals, and per established governance policies and procedures.
• Ensure technical and customer requirements for assigned projects are achieved.
• Develop and maintain required validation and project management documents.
• Conduct or participate in routine project reviews with Project Teams and Management
• Perform design work, layouts, sketches, concepts, etc. as needed for projects and/or plant layouts.
• Develop and/or review engineering change requests for modifications to processes, equipment and facilities.
• Troubleshoot and repair of all automation.
• Evaluate and maintain proper machine safeties to ensure employees are protected when operating any piece of automation.
• Ensure automation lines are meeting their targeted output and OEE by analyzing production data.
• Maintain quality finished product through proper maintenance and operation of all automation.
• Provide timely notification to shift leaders and program managers of maintenance and down time issues.
• Interfaces daily with engineering manager and shift support staff.
• Conforms with and abides by all regulations, policies, work procedures, instruction, and all safety rules.
• Performs other duties as assigned by management.
• Exhibits regular, reliable, punctual and predictable attendance.
• Automation includes – assembly machines/fixtures, label applicators, robots, end of arms, separators and test equipment. Any other equipment assigned by management.

• Associate's Degree In a relevant Engineering subject required or
• Bachelor's Degree In a relevant Engineering subject preferred

• Minimum 3 years Experience in medical device industry or other regulated industry required
• Minimum 3 years Experience in supporting technical project management preferred

• Background in medical devices/pharmaceutical would be a plus.
• Knowledge of quality systems requirements, FDA Quality System Regulation, cGMP and relevant ISO standards

5%: Up to 13 business days per year

Light-Exerting up to 20lbs/9kg of force frequently, and/or negligible amount of force frequently constantly to move objects.

• Must be able to work a 40-hour work week, plus overtime and/or irregular hours as required to complete assignments. May stand or sit for extended periods of time. Must transport oneself to and from other areas of the facility and travel to other divisions when necessary. Must have good visual acuity. If specifically necessitated by customer requirements, must be able to see with or without corrective lenses and distinguish color differences for product and safety issues.
• Medical Device manufacturing requires strict adherence to standards. Working environment is a manufacturing facility, which houses plastic injection molding machines. Must tolerate fumes and particulate generated from various plastics. Work areas are equipped with adequate lighting, cooling/heating and equipment that are in a good working condition. Must work constructively in an environment that may always be stressful due to competing resources while maintaining company confidentiality.

West embraces diversity and equality of opportunity. We foster an environment where all individuals are safe, treated fairly, valued and respected. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, disability status or other applicable legally protected characteristics. Where permitted by law, employment with West Pharmaceutical Services, Inc. or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of post-offer background screening and/or drug screening.

We are seeking a qualified
Electrician
to join a leading engineering team, supporting the maintenance, repair, and installation of electrical systems within manufacturing, industrial, or commercial environments. The successful candidate will work on a wide range of electrical equipment, ensuring safety, compliance, and operational reliability.

Key Responsibilities:

• Install, maintain, and repair electrical systems, wiring, and equipment.
• Diagnose electrical faults and carry out troubleshooting and repairs on production, facility, and utility systems.
• Read and interpret electrical schematics, technical drawings, and manuals.
• Ensure all work complies with relevant safety standards and electrical regulations (e.g., ETCI, RECI).
• Support commissioning and testing of new installations or upgrades.
• Maintain accurate records of work performed, parts used, and compliance checks.
• Collaborate with engineering, maintenance, and production teams to resolve electrical issues.
• Participate in continuous improvement and safety initiatives.

Requirements:

• Recognized electrical trade qualification (e.g., QQI Level 6, Electrical Craft Certificate, or equivalent).
• Minimum 3 years' experience as an electrician in industrial, manufacturing, or commercial settings.
• Strong fault-finding and problem-solving skills.
• Experience with automated systems, PLCs, or instrumentation is an advantage.
• Good communication and teamwork abilities.
• Commitment to safety and compliance.
• Flexibility to work shifts or respond to call-outs if required.

Desirable:

• Additional certifications in areas such as instrumentation, automation, or safety systems.
• Experience with building management systems, emergency lighting, or fire alarm systems.

Salary & Benefits:

• Salary Range: negotiable depending on the level (entry level - mid and senior level)
• Overtime, shift, and call-out premiums where applicable.
• Pension scheme, health insurance, and training opportunities.

To Apply:

Send your CV and a brief cover note outlining your relevant experience.

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 115,000 colleagues serve people in more than 160 countries.

In Ireland, Abbott has been operating since 1946, employing over 6,000 people across ten sites, including:

• Six manufacturing facilities in Clonmel, Cootehill, Donegal, Longford, and Sligo
• A third-party manufacturing management operation in Sligo
• Commercial, support operations, and shared services in Dublin and Galway

Abbott Ireland Diagnostic Division – Longford

The Longford facility plays a vital role in meeting the growing global demand for diagnostic testing in areas such as infectious disease, cancer, thyroid, and cardiovascular diseases.

Located in the heart of Ireland's midlands, Longford is surrounded by natural beauty including the River Shannon, Lough Ree, and the Royal Canal. The county offers a vibrant mix of communities, rich history, and a wide range of amenities, festivals, cultural events, and recreational activities.

Primary Function

The Manufacturing Manager is responsible for ensuring that the Longford facility meets its customer, regulatory, financial, and safety goals through the effective management of manufacturing and testing operations. This role supports new product and process transfers and leads strategic change initiatives to drive continuous improvement across the site.

Key Responsibilities

• Lead and manage assigned manufacturing and support functions within Operations
• Ensure major projects are delivered on time and within budget
• Maintain product availability and meet customer requirements for diagnostic reagents
• Drive timely completion of non-conformance investigations and CAPA activities
• Promote a culture of continuous improvement in safety, quality, and performance
• Optimize human resources through effective communication, teamwork, and engagement
• Ensure compliance with GMP, HR, safety, financial, and quality procedures
• Stay current with technical and manufacturing developments to maintain regulatory compliance
• Manage collaboration between Longford Operations and other Abbott sites
• Ensure quality standards are met for internal and external audits and customer expectations
• Support strategic planning and execution of operational changes
• Maintain operational task lists and project plans (e.g., ETMS TO DO LIST)
• Conduct business in compliance with EHS laws and Abbott global standards

Supervisory / Management Responsibility

• Direct supervision and leadership of manufacturing teams
• Responsible for team performance, development, and motivation

Education & Experience

• A relevant third-level qualification (e.g., Engineering, Science, or related discipline)
• Minimum 5 years' experience in a regulated manufacturing environment (Medical Device or Diagnostics preferred)
• Minimum 3 years' experience in people management and team motivation
• Strong communication and problem-solving skills
• Familiarity with regulatory requirements and quality systems

Accountability

• Accountable for the performance and compliance of assigned operations
• Decision-making within agreed product availability and performance goals
• Operates with general guidance from senior management
• Annual goals and performance reviews conducted with the Site Director

Connect with us at or , on LinkedIn at , on Facebook at and on Twitter @AbbottNews.

Manufacturing Operative – Assembly

Wilker Auto Conversions | Clara, Co. Offaly

€30,000 – €5,000 per year | Full-time | On-site

Build vehicles that make a difference with Wilker Auto Conversions

We're seeking a Manufacturing Operative – Assembly to join our growing production team. At Wilker, you'll help craft high-performance vehicles for emergency services, mobility solutions, and specialist conversions.

Why join Wilker?

• Competitive salary: €3 00 – €3 00 depending on experience
• Early finish Fridays: Wrap up by 1pm
• On-site parking and accessible location
• Career growth and development opportunities
• Supportive, inclusive culture – we welcome diverse talent

About the Role – Assembly Focus

As a Manufacturing Operative – Assembly, you'll work hands-on with a variety of materials to build and fit out custom vehicles. Experience in purpose-built vehicle assembly, cabinetry, or carpentry will be highly regarded.

What You'll Do:

• Install flooring, wall skins, cabinetry, windows, seating, and fabricated parts
• Fit sub-assembled systems and components
• Work from technical drawings and assembly specifications
• Collaborate with production teams to maintain high safety and quality standards

What You'll Bring:

• Fit-out or general manufacturing/building experience
• Skills such as panel screwing, bonding/gluing, and bolting
• Background in automotive, cabinetmaking, or carpentry is advantageous
• Attention to detail and a proactive, collaborative approach

Join Wilker and be part of a team building world-class specialist vehicles. Apply today

INDHP

Job Type: Full-time

Pay: €30,00 0- ,000.00 per year

Benefits:

• On-site parking
• Sick pay

Application question(s):

• Where do you currently reside?
• Do you hold an full Irish drivers license?

Work authorisation:

• Ireland (required)

Work Location: In person

PennEngineering is a global leader in the manufacturing of specialty fasteners and provide quality, value added products and services to our customers from our manufacturing and technical facilities around the world.

We are now seeking skilled manufacturing Operators with an interest in Engineering who want to become part of a highly motivated team based in our Galway manufacturing plant.

This is a hands-on role that would suit candidates with a good mechanical aptitude, a certificate in mechanical engineering, a trade certificate or equivalent training.

Our Shift Pattern:

We operate a 39 hour week / 4 Night rotation.

Week 1: Monday - Thursday 9.15pm - 7.30am

Week 2: Tuesday - Friday 9.15am - 7.30pm.

Responsibilities

• Learn and progress your knowledge of Cold Forming and Cold Heading manufacturing through on the job training and our dedicated training programmes.
• Operate, troubleshoot, setup and changeover mechanical fastener manufacturing machines.
• Ensure smooth and efficient running of high-volume production machinery.
• Work to production metrics and standard operating procedures to meet customer requirements.
• Ensure high quality product through quality Inspection of parts with precision and measuring tools.
• Work with quality/engineering and operations departments on continuous improvement & development programmes.
• Compliance with all Health & Safety regulations.

What we are looking for:

• Good mechanical aptitude & problem-solving skills.
• Ability to work in a fast paced and high-volume manufacturing environment.
• Basic mathematical skills
• Ability to effectively communicate in the English language
• Excellent attention to detail.
• A good mechanical aptitude, a certificate in mechanical engineering, a trade certificate or equivalent training.
• Ability to follow verbal and written instructions.
• A team player mindset and a willingness to learn a new skillset
• Relevant manufacturing experience and shift flexibility required.

Benefits:

• Starting rate of €12.93 per hour increasing as you become trained.
• Quarterly Bonus Scheme.
• Shift premium.
• Flexible shifts that offer work / life balance.
• Graded Pay Structure – Advance your salary as you grow your knowledge and skillset through our graded training programme
• Permanent contract.
• Healthcare benefit after one years' service
• Service days
• Pension
• Educational Sponsorship Programme & Internal Training Programmes

Job Types: Full-time, Permanent

Pay: From €15.00 per hour

Work Location: In person

At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world.
Job Overview
The NPD (New Process Development) Manufacturing Engineer will be responsible for leading project-related Engineering activities within NPD and providing Engineering support to the Manufacturing department during the new product introduction cycle. In addition to this, the NPD Manufacturing Engineer will be responsible for the development of both existing and new process technologies as required by new products and prototypes.

*Job Requirements *

• Work as part of the NPD team to drive product and process improvements.
• Manage new designs through product lifecycle into manufacturing.
• Work closely with Subject Matter Experts in the business to ensure all new products fit within Creganna Medical's existing manufacturing capability.
• Work closely with Lean and Operations teams to ensure that any new processes developed meet world-class manufacturing standards.
• Display customer focus always and be accountable for quality and timeliness of own work.
• Manage a variable workload across different projects to meet NPD requirements.
• Design and introduce manufacturing processes for new products to meet the demands of productivity and quality.
• Ensure that complete and effective validations are carried out on all processes before transferring to manufacture including IQ, OQ, PQ & PPQ.
• Identify and put in place permanent and effective technical/system solutions to problems.
• Maintain high quality/compliance standards in line with Medical Device manufacturing requirements within Creganna Medical.
• Applying Lean principles to identify and develop improvements that increase key process metrics of yield, throughput and productivity.
• Investigate new process technologies and evaluate potential competitive advantage and the cost-benefit of introduction.
• Manage external relationships with technology providers/suppliers.
• Ensure that all Health, Safety and Environmental requirements are fulfilled.

*What your background should look like
Qualifications *

• Level 8 Engineering degree, or equivalent qualification.
• 2+ years' experience in a similar role.

Key Requirements

• Strong mechanical background with a good working knowledge of metals processing a distinct advantage. Previous experience with laser cutting, laser welding or machining processes a distinct advantage.
• Ability to develop process settings/windows using scientific methodology.
• Knowledge of Six-Sigma methodology, problem-solving tools and Lean Manufacturing principles.
• A demonstrated ability to solve problems with innovative and cost-effective solutions.
• CAD, Solid works, Creo and Minitab experience preferable.
• Experience working in a high-volume production environment would be beneficial.
• Computer literate and familiar with all Office software packages.
• Motivated to work on own initiative and the ability to make and implement decisions.
• Excellent communication, planning and organizational skills

#jobsEMEANR
*Competencies *
Values: Integrity, Accountability, Inclusion, Innovation, Teamwork

About Te Connectivity
TE Connectivity plc (NYSE: TEL) is a global industrial technology leader creating a safer, sustainable, productive, and connected future. Our broad range of connectivity and sensor solutions enable the distribution of power, signal and data to advance next-generation transportation, energy networks, automated factories, data centers, medical technology and more. With more than 85,000 employees, including 9,000 engineers, working alongside customers in approximately 130 countries, TE ensures that EVERY CONNECTION COUNTS. Learn more at , ,

What Te Connectivity Offers
We are pleased to offer you an exciting total package that can also be flexibly adapted to changing life situations - the well-being of our employees is our top priority

• Competitive Salary Package
• Performance-Based Bonus Plans
• Health and Wellness Incentives
• Employee Stock Purchase Program
• Community Outreach Programs / Charity Events
• Employee Resource Group

IMPORTANT NOTICE REGARDING RECRUITMENT FRAUD
TE Connectivity has become aware of fraudulent recruitment activities being conducted by individuals or organizations falsely claiming to represent TE Connectivity. Please be advised that TE Connectivity
never requests payment or fees
from job applicants at any stage of the recruitment process. All legitimate job openings are posted exclusively on our official careers website at , and all email communications from our recruitment team will come
only from actual email addresses ending in
. If you receive any suspicious communications, we strongly advise you not to engage or provide any personal information, and to report the incident to your local authorities.

Across our global sites and business units, we put together packages of benefits that are either supported by TE itself or provided by external service providers. In principle, the benefits offered can vary from site to site.

WG
NSTAR is a dynamic and growing company with a global footprint. Primarily focused on the semiconductor industry, we provide a platform for you to expand your career with knowledge gained on the job training, and tailored development. We know we need talented people like you that hold similar values, which is why we do not put limits on learning, development, industry, and personal growth. Start your path to a
WG
NSTAR career today

The Purpose of the Role
As a Manufacturing Technician, you will be supporting the Customer in key areas throughout the manufacturing process. Your role will be centered around adhering to facility standard operating procedures with a focus on safety and quality.

Person Specification

• You enjoy technical problem solving, whether this be DIY projects or maintenance and repairs on your car or bike
• A strong team player
• Have excellent organisational and time keeping skills
• Ability to adapt to different tasks
• You are looking for a new challenge and to develop your career

Work Schedule
Compressed Work Week, 4 days on 3 days off, 3 days on 4 days off (7 days over a 14 day period), 12-hour shifts (day & night including weekends).

Principal Duties And Responsibilities

• Handling, transporting, and recording critical materials within the factory
• Maintaining cleanroom and company protocols
• Ensuring safety and quality standards are maintained
• Performing quality checks in line with process specifications
• Using MS Office and in-house computer system as required

Role Requirements

• Ability to work in a controlled cleanroom environment, which will involve the wearing of a gown and relevant personal protective equipment
• 100% compliance with all safety and protocol specs and regulations

Physical Requirements

• Have strong physical stamina to have the ability to stand, stoop, walk and reach for the duration of a 8-hour shift (breaks excluded)

Benefits Of Working With WGNSTAR

• Discounted rates of on-site facilities
• Free on-site car parking
• Reward & Recognition Programme
• Employee Assistance Programme
• Learning and development
• Opportunities for career progression

This job description is intended to convey information essential to understanding the scope of the job and the general nature and level of work performed by job holders within this job. This job description is not intended to be an exhaustive list of qualifications, skills, efforts, duties, responsibilities or working conditions associated with the position.

WGNSTAR does not require assistance from Recruitment Agencies. Thank you.

Equal Opportunities Employer
WG
NSTAR is an Equal Opportunity Employer in accordance with The Employment Equality Acts.
WG
NSTAR places strong emphasis on equal employment, encourage diversity in the workplace, and apply an open-door policy for inclusion of all employees. Our diversity program encourages people from any gender, background, ethnicity, culture, education, and experience to join the company and more importantly build a career through employee development.

Additional Locations: N/A

Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance

At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we'll help you in advancing your skills and career. Here, you'll be supported in progressing – whatever your ambitions.

Purpose Statement

To support the engineering and implementing of highly capable & effective manufacturing processes to meet business goals and objectives.

Key Responsibilities

• To support the key activities utilized in quality, service & cost improvements in the Operations Engineering Cycle to meet key business objectives.
• To support a prioritised approach in Value Centred Engineering to achieve the key opportunities in quality, service and cost.
• Production line monitoring and the identification and quantification of process problems, along with subsequently implementing the necessary improvements and/or controls.
• Liaising with the Quality and Operations functions in pursuit of achieving the quality and S&OP targets for each given area.
• Participation in cross-functional projects works as dictated by the emerging business needs.
• Taking direction from Manufacturing Engineer II's and Senior Engineer's as to how best to deploy resources and effort on the operations floor.
• Actively seek ways and means of increasing efficiency, productivity, yield and space utilisation on the operations floor.
• Manage material risks, as identified by the business.
• Always Observe the Quality Management Systems requirements on site.
• Communicate regularly with the Product Builders regarding issues, concerns and watchouts on the lines.
• Work closely with our in-house Equipment Design & Engineering workshop in getting equipment/fixtures designed & fabricated.
• Development and implementation of appropriate supporting documentation which complies with Good Manufacturing Practices (GMP) in conjunction with other team members.
• Leading technical improvements under the site's continuous improvement program.
• Actively interfacing with cross-functional team members, always practicing good teamwork in support of day-to-day operating requirements.

Education & Experience

• Level 8 Honours Batchelors degree in a relevant Engineering or Science discipline.
• Strong communicator with excellent problem-solving skills.
• Teamwork & collaboration is a key competency for this role.
• Ideally experience of working in a regulated environment.

Requisition ID:

As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most – united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do – as a global business and as a global corporate citizen.

So, choosing a career with Boston Scientific (NYSE: BSX) isn't just business, it's personal. And if you're a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you

Work Flexibility: Hybrid

Purpose of Role:

The Manufacturing Engineer (ME) will provide engineering and process support to ensure successful implementation of 2D barcoding in line with EU MDR requirements.

This role will focus on supporting technical strategy execution, process validation, and operational readiness across both internal manufacturing and supplier sites.

Key Responsibilities:

• Support technical execution of 2D barcode implementation, including validation activities (VP, IQ, OQ, PQ).
• Partner with Quality Engineers (QEs) and Supplier Quality Engineers (SQEs) to assess and confirm laser marking equipment compatibility and process qualification at both supplier and internal sites.
• Assist in First Article Inspection (FAI) preparation, reviewing supplier provided verification data and ensuring compliance to marking requirements.
• Update and maintain manufacturing documentation (DCP, PFMEA, SOPs) to reflect new barcoding processes.
• Collaborate with operations teams to ensure inspection readiness (visual inspection, barcode verifier checks).
• Troubleshoot and provide technical support during initial marking trials and confidence runs.
• Support scrap management, label obsolescence, and carton switchovers as required for Go-Live phases.
• Actively contribute to risk assessments, ensuring process robustness and alignment with MDR and GMP requirements.

Required Skills & Experience:

• 2–4 years' experience in a regulated manufacturing environment (medical device preferred).
• Exposure to process validation and FAI/PPAP activities in a regulated environment.
• Familiarity with laser marking or UDI/2D barcoding processes desirable.
• Strong problem solving and root cause analysis capability (Six Sigma / Lean tools beneficial).
• Proven ability to work collaboratively with cross functional teams (QE, SQE, and Operations).

Travel Percentage: 10%