171 Manufacturing Trainee jobs in Ireland

Job Title: Manufacturing Engineer(Med Device Manufacture) Hours: Hybrid role 3 days on site with a 1pm Friday finish and free on-site gym.

39hr week offering flexitime Location: Galway Industry: Medical Devices Company information: Galway's world leading multi-national Medical device company Contact: To discuss email CV to or call Manufacturing Engineer: Medical Devices Galway's world leading medical device manufacturing company have available opportunities for EXPERIENCED Manufacturing Engineers to join their team.

Please send CV to to apply.

About the role: Purpose: To support a critical site-wide remediation program following an FDA 483 role offers a fantastic opportunity to work directly onsite, collaborating closely with manufacturing and quality teams to drive compliance improvements and process validation initiatives.

Hours of work: Monday-Friday 39hr week with a 1pm Friday finish.

Key Responsibilities: Partner with manufacturing process owners to identify and remediate compliance gaps.

Support manufacturing process validation activities (IQ/OQ/PQ).

Update quality system documentation and technical files to ensure audit readiness.

Drive closure of CAPAs and NCRs with effective corrective actions.

Provide clear and concise technical writing for quality and manufacturing procedures.

Collaborate cross-functionally with Quality, Manufacturing, and Regulatory teams to implement compliant solutions.

Qualifications & Experience: Bachelors degree in Engineering or Quality-related discipline.

25 years of experience in medical device manufacturing, quality, or remediation projects.

Strong knowledge of process validation (IQ/OQ/PQ) and CAPA/NCR management.

Proven technical writing and documentation skills.

Familiarity with 21 CFR Part 820 and ISO 13485 quality standards.

Excellent problem-solving skills with the ability to take a problem statement through to a compliant solution.

Must be available to work onsite in Galway.

Contact: Rachel Mc Mahon for more information Email:/ INDCRG Skills: IQ OQ PQ CAPA NCR

Manufacturing Engineer
**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**
Working within the core Engineering group, and reporting to the Senior Engineer, the Manufacturing Engineer - must be motivated in delivering improvements and making a positive difference to be successful in such a role, sharing a desire for excellence, a value for the company you are working for. You will have the ability to analyse data and complete root cause analysis as essential skills gained within the manufacturing environment. The Engineer will support Technicians in a Manufacturing environment and be responsible for supporting all engineering activity in areas of responsibility.
**Job Requirements**
+ Work with key business stakeholders and operations teams to build a continuous improvement environment that supports ongoing change and improvement initiatives.
+ Support the delivery of better value and greater efficiency through the identification and elimination of unnecessary complexity within Balloon forming processes and identification of simplified ways of working.
+ Identify and put in place permanent and effective technical / system solutions to quality and technical problems.
+ Implement equipment maintenance procedures for critical equipment.
+ Investigate new process technologies and evaluate potential competitive advantage and the cost-benefit of introduction.
+ Consistently meet customer requirements and commitment to excellence in performance and meeting deadlines.
+ Maintain high quality/compliance standards in line with Medical Devices manufacturing requirements within Creganna Medical, part of TE Connectivity.
+ Resolving quality and technical issues such that impact on product supply to customers is minimized.
+ Maintain high quality / compliance standards in line with Medical Devices manufacturing requirements within Creganna Medical, part of TE Connectivity.
+ Work as part of Production Support team to drive product and process improvements/developments.
+ Update Manufacturing procedures, specs as required through change control process.
+ Ensure that all Health, Safety and Environmental requirements are fulfilled.
+ Projects - identify and implement continuous improvement projects to reduce scrap across the business unit.
+ New equipment introductions - EIQ/EOQ, DOE & Process OQ/PQ Validations.
**What your background should look like**
**Qualifications**
+ Level 8 Polymer degree, or equivalent.
+ Preferably a minimum of 1 years' experience in a similar role.
**Key Requirements**
+ Experience in Med Device distinct advantage.
+ Demonstrated experience in Process troubleshooting
+ Designed and validated new manufacturing methods and equipment in collaboration with vendors
+ Must be able to plan, organize, and implement multiple concurrent tasks and projects.
+ Jigs & Fixtures design and maintenance experience would be an advantage.
+ Demonstrate a practical understanding of Lean Manufacturing principles and statistics.
+ Demonstrate operating knowledge of Minitab software, would be an advantage.
+ SolidWorks /AutoCAD skill would be an advantage.
+ Demonstrate a dynamic, motivated & flexible approach to work with results-oriented attitude.
+ Excellent communication, planning and organisational skills.
+ Knowledge of ISO & FDA compliance.
**#jobsEMEANR**
**#LI-ONSITE**
**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 and on LinkedIn ( ,Facebook ( ,WeChat, ( Instagram andX (formerly Twitter). ( 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 te.com/careers, and all email communications from our recruitment team will come **only from** **actual** **email addresses ending in @te.com** . 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.
Location:
GALWAY, G, IE, H91 VN2T
City: GALWAY
State: G
Country/Region: IE
Travel: 10% to 25%
Requisition ID:
Alternative Locations:
Function: Engineering & Technology
TE Connectivity and its subsidiaries, affiliates, and operating units (collectively, the "Company") is committed to providing a work environment that prohibits discrimination on the basis of age, color, disability, ethnicity, marital status, national origin, race, religion, gender, gender identity, sexual orientation, protected veteran status, disability or any other characteristics protected by applicable law or regulation.

**Who we want**
+ **Performance** : Deliver high quality products.
+ **Team Player** : Build positive relationships with others to achieve common goals.
+ **Reliable** : Manage time to effectively get the job done.
A Manufacturing Operator effectively builds the products manufactured by Stryker to the required quality standard
**What you will do**
+ Responsible for manufacturing product in accordance with the relevant Stryker manufacturing procedures and relevant quality standards
+ Participation in continuous improvement programmes or team projects to enhance our quality customer service and cost
+ Monitor and verify quality in accordance with workmanship standards and operating procedures
+ Adhere to procedures in relation to production methods, completion of documentation, current Good Manufacturing Practices and safety requirements
+ Provide cross training to other employees
+ Contribute as part of a team in achieving the line core metrics
+ Build Quality into all aspects of their work by maintaining compliance to all quality requirements
**What you need**
+ Leaving Certificate, Trade or equivalent education level is required
+ Previous experience in production/ assembly roles is desirable
+ Basic mathematics and good English skills
+ Good communication skills
+ Willingness to work in a team and promote teamwork
+ Previous experience in production/ assembly roles is an advantage
+ The employee may be required to use protective clothing and safety equipment such as safety glasses and respirators, and the use of personal protective equipment (PPE)
*** Please note this is initially a 12 month fixed term contract based in our Model Farm Road location**
#IJ
This role will be posted for a minimum of 3 days.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.

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).
This role will be posted for a minimum of 3 days.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.

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).
This role will be posted for a minimum of 3 days.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.

**Who we are:**
Abbott has a presence in over 160 countries and has over 113,000 employees. Our new manufacturing facility in Kilkenny (R95 A02A) is Abbott's 7th manufacturing site in Ireland.
The facility is a centre for world-class engineering, quality, medical device manufacturing. We have been making a difference in the lives of Irish people since 1946.
**Abbott Ireland**
In Ireland, Abbott employs around 6,000 people across ten sites. We currently have seven manufacturing facilities located in Clonmel, Cootehill, Donegal, Longford, Kilkenny and Sligo and a third-party manufacturing management operation in Sligo. Abbott also has commercial, support operations and shared services in Dublin and Galway. We have been making a difference in the lives of Irish people since 1946.
**What is this position:**
As Manufacturing Technician you will provide technical support relating to equipment utilized in the manufacturing areas by repairing, maintaining, or modifying production equipment.
Monitoring machine output on the shift to and ensure all cells are running to cycle time, to meet specific targets.
**What You'll Be Doing:**
+ Install and equipment validation
+ Conducting scheduled maintenance, diagnosing, and troubleshooting faults
+ Perform skilled maintenance and repair such as mechanical, pneumatics, electrical systems
+ Lead on maintenance and/or process issues
+ Ability to interpret blueprints and schematics.
+ Certifies and train manufacturing associates in the production processes.
+ Identifies and implements corrective actions for manufacturing related issues.
**How does this role fit into the organisation:**
You will report to a process Engineering Manager on a team of approx. 20. Your team will include process engineers and manufacturing technicians.
**What we're looking for:**
+ Min level 6 qualification (Trade or Third level equivalent)
+ Electrical and mechanical skills are desired
+ Technical and fault-finding skills
**What's in it for you:**
+ Pension
+ Healthcare
+ Bonus
+ Life insurance
+ Disability insurance
+ Paid maternity leave
+ Parental leave
+ Adoptive leave
+ Flexible working
Connect with us at or , on LinkedIn at , on Facebook at and on Twitter @AbbottNews.
Abbott is an equal opportunities employer
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

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. To Apply Please forward your CV via the APPLY Now button below.

Manufacturing Technician - Thurles / Templemore My client has just launched a brand-new yeast production plant near Thurles/Templemore, transforming a dairy by-product into a sustainable, non-GMO animal feed. They're now looking for a Manufacturing Technician to join their growing team. This is a hands-on role where you'll play a key part in the day-to-day running of the facility and help shape the future of an exciting new venture. What You'll Be Doing (full training provided) Materials Handling - Receive, test, and manage raw materials and stock. Fermentation Runs - Operate and monitor yeast fermentation, including vessel setup, inoculation, controls, and cleaning. (Initially under close supervision until processes are fully refined). Process Monitoring - Record and track fermentation data to identify trends and improvements. Concentration - Operate, oversee, and clean the centrifuge used to concentrate fermented material. Drying & Bagging - Monitor drying, milling, and bagging of yeast biomass into powder. Cleaning - Utilise CIP skid to maintain high hygiene standards. Maintenance - Carry out routine maintenance tasks as required. Quality Assurance - Follow SOPs to meet quality, safety, and production standards. Collaboration - Share results, flag issues, and work closely with colleagues to keep things running smoothly. What We're Looking For Detail-focused with strong problem-solving skills. A flexible, positive communicator who enjoys learning new skills. Comfortable with shift work. Adaptable to changing priorities in a fast-moving environment. What's in It for You Salary up to €35K DOE. Be part of a start-up where your ideas and input truly count. Work within a flat structure and supportive, close-knit team. Ready to Apply? If you're looking for your next step as a Manufacturing Technician and want to be part of a ground-breaking start-up from day one apply now and help shape the future of sustainable food production! Skills: Tipperary Manufacturing Technician General Operative

Manufacturing Engineer Dundalk €40k - €45k Vickerstock is currently working in partnership with one of the Irelands most succesful manufacturing firms to assist them with the recruitment of a Manufacturing Engineer. You will work with some of the most talented individuals in the industry to assist with the lean manufacturing practises across the site. Your key responsibilities as a Manufacturing Engineer Lead the day-to-day delivery of the CI process through the site functions. Be an integral member of a team of multi-skilled stream experts to deliver and exceed targeted KPI's, focussed on a comprehensive fault finding and analysis process. Support team with root cause identification and solutions designed to prevent repeated failures using lean tools and techniques. Liaise with department streams through Kaizens, understanding issues and setting plans to resolve. Carry out technical reviews with PSM & Engineering Lead on core systems and work with suppliers to optimise across site Update / maintain all asset documentation as required such as machine settings, manuals, PLC back-ups, labelling & PPM schedules resulting from CI works. Document and train maintenance Standard Work and Standard Operating Procedures arising from CI works. Apply analytical data techniques to prioritise work in conjunction with the Production Streams. As a Manufacturing Engineer, ideally you will have. An industry recognised qualification in Mechanical or Electrical Engineering At least 2 years' experience in manufacturing environment Proven problem solving skills. What we hope you will do next; Contact Warren Watson to discuss this in absolute confidence or send an updated CV via the link on the page. By applying for this role, you accept the terms of processing, please find our privacy policy on our website. As an experienced specialist senior engineering and manufacturing recruitment professional with 7 years' experience; I personally specialise within the recruitment of Lean Engineers at all levels across Ireland. If you are interested in this vacancy, or work within Lean Engineering / Manufacturing in Ireland, then please apply with your CV to me for consideration - (You can also find and connect with me on LinkedIn) Skills: Manufacturing Engineer Process Engineer Lean.