140 Manufacturing Technician 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.

About the job - Manufacturing Technician

Permanent employee, Full-time

An exciting opportunity has opened for a
Manufacturing Technician
to join a leading organisation in the
biopharmaceutical manufacturing sector
. This role is ideal for someone who wants to develop their career in a regulated GMP environment while working with innovative technologies.

Key Responsibilities

• Carry out GMP manufacturing and improvement activities to support production.
• Maintain cleanroom standards, ensuring compliance with GMP, GDP, and Data Integrity.
• Manage materials and bioprocessing activities within ERP systems.
• Support safety and quality investigations, driving continuous improvement.
• Contribute to a safe, compliant, and inspection-ready manufacturing environment.

Qualifications

• Experience in a GMP manufacturing environment (preferred but not essential).
• Strong attention to detail and adherence to cleanroom behaviours.
• Good communication skills (written and verbal).
• Comfortable working rotating shifts (early, late, and potential night shifts).
• Competency with IT systems (e.g., Microsoft Office).

What We Offer

• Permanent, full-time opportunity within advanced biopharmaceutical manufacturing.
• Structured training and career development in a regulated GMP environment.
• Exposure to innovative technologies and processes.
• Supportive team culture with a focus on safety, quality, and improvement.
• Competitive package including
  shift premium
  for late and night work.

Position Title:

Manufacturing Technician

Location:

Athlone, Co. Westmeath

Key Responsibilities:

• Operate, maintain, and troubleshoot manufacturing equipment to ensure optimal performance and minimal downtime.
• Diagnose and resolve mechanical issues using problem-solving techniques to maintain production efficiency.
• Conduct routine maintenance and calibration of equipment in compliance with industry regulations.
• Ensure adherence to all safety, quality, and regulatory standards within a manufacturing environment.
• Collaborate with cross-functional teams, including engineering and quality assurance, to improve processes and equipment performance.
• Maintain accurate documentation and reports related to equipment performance, maintenance activities, and any deviations.
• Support continuous improvement initiatives and contribute to process optimization projects.

Qualifications:

• Certificate or Diploma in Mechanical Engineering or a related discipline.
• Minimum of 3 years of experience in a regulated manufacturing environment.
• Strong problem-solving skills with the ability to troubleshoot and resolve mechanical issues efficiently.
• Experience working in a GMP, ISO, or similar regulated manufacturing setting.

Preferred Qualifications:

• Experience in the medical device, or precision manufacturing industries.
• Knowledge of lean manufacturing, Six Sigma, or similar process improvement methodologies.
• Strong technical aptitude with hands-on experience in mechanical systems, automation, or CNC machinery.
• Excellent communication and teamwork skills to collaborate effectively within a multidisciplinary environment.

Job Type: Full-time

Benefits:

• Company events
• On-site parking
• Private medical insurance

Education:

• Advanced/Higher Certificate (preferred)

Experience:

• Manufacturing: 3 years (preferred)

Work authorisation:

• Ireland (required)

Work Location: In person

05 - Operations Engineering Support 2

Req ID:

Remote Position: No

Hiring Manager: Caroline Scully

Band: 05

Region: Europe

Country: Ireland

State/Province: Galway

City: Galway

General Overview

Functional Area:
ENG - Engineering

Career Stream:
OPE - Operations Engineering

Role:
Technical Support 2

SAP Short Name:
TS2

Job Title:
Operations Engineering Support 2

Job Code:
TS2-ENG-OPS

Job Level:
Band 05

Direct/Indirect Indicator:
Direct

Summary
The Equipment Maintenance Technician is responsible for the set-up, installation, maintenance and support of automated equipment ensuring optimum performance and the achievement of operational goals. The Equipment Maintenance Technician works closely with teams to resolve manufacturing issues and constraints while implementing safe and robust solutions to improve overall efficiency through improvement projects around run rate increase, cycle time gains, yields and quality.

This position for the day 8 AM - 8 PM Days.

This position will report to the Team Leader.

Detailed Description

• Repairs and troubleshoots electro/mechanical equipment failures.
• Schedules and performs preventative maintenance procedures.
• Helps move, install, set-up and refurbish equipment.
• Maintains accurate and up-to-date maintenance documentation.
• Records significant downtime issues and resolutions in appropriate databases.
• Interacts with other departments as required to co-ordinate equipment repairs.
• Works proactively to ensure performance targets are met; Yield/quality (using SPC/SQC)/production outs/up-time /process stability.
• Communicates potential problems that may affect capacity and quality to the Business Unit Team Leader as well as across zones/work areas where necessary.
• Attends pass-downs as required and provides status updates.
• Provides detailed inputs into failed spare parts management process.
• Supports Process Engineers to ensure Continuous Improvements are ongoing.
• Trains and assists other Technicians and Operators.

Knowledge/Skills/Competencies

• Strong knowledge of the setup, operation, and maintenance of specific equipment sets used in manufacturing processes.
• Strong troubleshooting/Problem solving skills.
• Demonstrates a high level of technical ability, with hands on approach to solving technical issues.
• Excellent written and verbal communication skills.
• Good interpersonal skills and ability to work as part of a team.
• Commitment to achievement of manufacturing excellence.
• High level of flexibility: shift changes / training courses / preventative maintenance and Project support.
• Ability to work on own initiative, is self-driven.
• Resourceful, hands-on, enjoys a challenge.
• Works well under pressure.

Typical Experience

• 2 - 4 years+ experience as a Technician in a high volume automated environment.
• Minimum Cert./Diploma/Senior Trades in Electrical/Mechanical Engineering or equivalent.
• Working knowledge of PLCs, Motor drives, pneumatic and hydraulic components is an advantage.

Celestica is an equal opportunity employer. All qualified applicants will receive consideration for employment and will not be discriminated against on any protected status (including race, religion, national origin, gender, sexual orientation, age, marital status, veteran or disability status or other characteristics protected by law).

At Celestica we are committed to fostering an inclusive, accessible environment, where all employees and customers feel valued, respected and supported. Special arrangements can be made for candidates who need it throughout the hiring process. Please indicate your needs and we will work with you to meet them.

Manufacturing Technician – Abbott Kilkenny

Empowering Innovation in Medical Device Manufacturing

Abbott is a global healthcare leader operating in over 160 countries with more than 113,000 employees. In Ireland, we've been improving lives since 1946, with over 6,000 employees across ten sites — including seven cutting-edge manufacturing facilities.

Our newest site in Kilkenny is a hub of advanced engineering, precision manufacturing, and innovation. As part of our commitment to Industry 4.0, we're integrating smart technologies, data-driven decision-making, and automation to deliver world-class healthcare solutions.

About the Role

As a Manufacturing Technician, you'll be at the forefront of our smart manufacturing operations — supporting high-performance equipment, driving process excellence, and contributing to a culture of innovation. You'll join a growing, multidisciplinary team focused on delivering quality, efficiency, and continuous improvement.

What You'll Be Doing

• Install, validate, and optimize manufacturing equipment
• Perform predictive and preventive maintenance using digital tools
• Diagnose and resolve faults across mechanical, pneumatic, and electrical systems
• Lead troubleshooting and root cause analysis using data insights
• Interpret technical drawings, schematics, and digital documentation
• Train and certify operators in advanced production processes
• Identify and implement process improvements aligned with lean and Six Sigma principles

What We're Looking For

• Minimum Level 6 qualification (Trade or Third-level equivalent)
• Strong electrical and mechanical aptitude
• Proven fault-finding and problem-solving skills
• Experience with automation, sensors, or PLCs is a plus
• A proactive, detail-oriented mindset with a passion for innovation
• Ability to work independently and collaboratively in a fast-paced environment

What's in It for You

• Competitive salary and performance-based bonus
• Pension and comprehensive healthcare
• Life and disability insurance
• Paid maternity, parental, and adoptive leave
• Flexible working options
• Access to cutting-edge technologies and continuous learning
• A supportive, inclusive workplace where your ideas matter

The Right Fit

This role is ideal for someone who thrives in a technology-driven, high-performance environment. You're disciplined, dependable, and motivated by precision and progress. You bring a strong sense of ownership, a commitment to quality, and a desire to grow with a company that's shaping the future of healthcare.

Ready to power the next generation of medical manufacturing?

Apply now and be part of something extraordinary.

Purpose of Job

The main purpose of the Manufacturing Technician is to perform manufacturing and improvement activities in accordance with Good Manufacturing Practice to support the manufacture of Advanced Therapy Medicinal Products (ATMP).

Major Activities

• Responsible for performing manufacturing and improvement activities in accordance with Good Manufacturing Practice to manufacture ATMP.
• Responsible for identifying, reporting and supporting health and safety issues and investigations, and responsible for identifying potential health and safety improvements.
• Responsible for maintaining own work and work area in an inspection-ready state at all times.
• Responsible for driving personal development, seeking opportunities to grow and expand additional capabilities.
• Responsible for communicating professionally, accurately and in a timely manner with team members and other stakeholders.
• Responsible for identifying, collaborating and delivering continuous improvements within the manufacturing area to improve safety, quality and flow.
• Responsible for identifying, reporting and supporting quality issues and investigations.
• Responsible for ensuring that individual and co-worker work complies with GMP, Data Integrity and Good Documentation Practice (GDP) and is undertaken in accordance with applicable procedures.
• Responsible for ensuring that the necessary training is undertaken in a timely and GMP compliant manner before the task is undertaken.
• Responsible for ensuring that any GMP documentation assigned is closed in a timely manner, right-first time and in compliance with MeiraGTx procedures.
• Responsible for ensuring the facility and materials are sanitised, monitored and controlled adequately to prevent contamination or cross-contamination.
• Responsible for movement and preparation of materials required for bioprocessing and support activities inclusive of their management within the Enterprise Resource Planning system.
• Responsible for ensuring materials used within manufacturing are correct, clean, appropriate and in place ready for manufacture to the agreed schedule.

Key Performance Indicators

• Safe working of self and with others.
• Compliance with GMP requirements including Data Integrity.
• Excellent cleanroom behaviours.
• Timely closure of GMP commitments.
• High standards of professional conduct including timeliness, teamwork, respect for others, and commitment.
• All training completed prior to undertaking a task, with no overdue training.

Key Job Competencies

• Good Documentation Practice - Operates to appropriate manufacturing practices and procedures to produce and complete documentation of the highest standard.
• Cleanroom behaviours – Operates to a high standard of hygiene and technique within cleanrooms to maintain the required level of cleanliness for ATMP manufacturing.
• Motivation - demonstrates persistence and overcomes obstacles; strives for excellence and demonstrates consistent pride in own work.
• Professionalism - approaches others in a tactful manner; reacts well under pressure; treats others with respect and consideration regardless of their status or position; accepts responsibility for their own actions; follows through on commitments.
• Quality Improvement - looks for ways to improve and promote quality; demonstrates accuracy and thoroughness.
• Innovation - meets challenges with resourcefulness; generates suggestions for improving work; develops innovative approaches and ideas.
• Oral Communication - speaks clearly; listens and gets clarification; responds well to questions; demonstrates good presentation skills; participates effectively in meetings.
• Written Communication - writes clearly and informatively; edits work for spelling and grammar; varies writing style to meet needs; presents numerical data effectively; able to read and interpret written information.

Job Responsibilities

• Responsible for GxP compliance within designated processing areas.
• Accountable for safety of self and team within designated processing areas.

Experience / Professional Background

• Fluent English language (written and oral).
• Competency and familiarity with basic IT systems (e.g. Microsoft Office, etc.).
• Previous experience in a GMP manufacturing environment (preferred not mandatory).

Shift Outline

The role entails shift work as follows:

• Early Shift: 07:00 – 15:00pm
• Late Shift: 15:00-23:00pm
• (Rotating shift pattern; week 1 Early, week 2 lates, week 3 Early, week 4 lates etc .).
• You many also be temporarily required to work a regular day shift 08:30 – 16:30pm or a 12-hour day shift 07:00-19:00pm between the rotating shift patterns.
• As part of this role, you may also be required to work night shifts therefore in accepting the role you acknowledge that you may be required to work night shifts (12 or 8 hours depending on roster).
• Compensation for the above Shift Patterns, including the potential night work, will be in the form of a monthly Shift Premium.