151 Manufacturing Engineer jobs in Ireland

Working at Freudenberg: "We will wow your world" This is our promise. As a global technology group, we not only make the world cleaner, healthier and more comfortable, but also offer our 52,000 employees a networked and diverse environment where everyone can thrive individually. Be surprised and experience your own wow moments.

Freudenberg Medical is a trusted Contract Manufacturing Organization (CDMO) partner, delivering high-quality solutions from ideation and market launch to volume production for medical device and pharmaceutical companies. With proven expertise in materials and technologies, Freudenberg Medical offers an extensive range of vertically integrated capabilities: precision molding and extrusions, complex catheters, hypotubes, and coatings.

Some of your Benefits

Flexible Work Models

Health Insurance

Company Pension

Personal Development

Education Reimbursement

Carrick-on-Shannon (Co. Leitrim)

On-Site

VistaMed Ltd.

Join our team as a:

MANUFACTURING ENGINEER (ASSEMBLY)

Responsibilities

• Join a fast-growing global medical device company where you'll play a hands-on role improving how life-changing products are made.
• Get involved in real problem solving - support investigations into process issues, non-conforming materials, and customer feedback.
• Take ownership of your processes, helping to optimise production and maintain world-class quality standards.
• Work side-by-side with experienced Engineers, Technicians, and Operators, learning from the best and contributing your own ideas.
• Help design and improve manufacturing layouts and workflows, making production smoother, safer, and more efficient.
• Support quality and continuous improvement projects, including MRB, CAPA, and Lean initiatives that drive measurable results.
• Collaborate with R&D and NPI teams, gaining exposure to new product introductions and early-stage process design.
• Grow your career in a supportive, development-focused environment, with clear progression opportunities as the company continues to expand.

Qualifications

• A Bachelor's Degree in Polymer, Science, Biomedical, or Mechanical Engineering - or strong experience in a Process or Assembly Technician role within a medical device environment.
• Experience (or strong exposure) to cleanroom manufacturing, validation, process control, and continuous improvement.
• A solid understanding of Lean and process improvement principles - or the enthusiasm to develop these skills on the job.
• Students, graduates, and apprentices are welcome to apply - you'll be fully supported and paired with an experienced mentor to help you grow your technical skills.
• Associate and Junior Engineers will work closely with senior team members, gaining hands-on experience and exposure to a wide range of processes.
• More experienced candidates (4+ years) may be considered for a Senior Engineer position, depending on experience and capability.
• A Lean Systems Green Belt (LSGB) or Six Sigma Green Belt (SSGB) certification is a plus – but not essential; we value drive, curiosity, and a willingness to learn.

The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law.

Additional Information

Emma Reynolds

Manufacturing Engineer

Location:
Shannon, County Clare

About the Role

We are proud to be representing a leading organisation with a strong global presence and an established base in Shannon, Co. Clare, is seeking a skilled
Manufacturing Engineer
to strengthen its engineering team. This is a key position within the company, suited to candidates with experience in fast-paced, multinational environments and a passion for driving improvements in manufacturing processes.

Main Responsibilities

• Deliver engineering support to both internal production teams and external customers/suppliers.
• Contribute to the planning and design of new processes that can be seamlessly introduced into production.
• Oversee the manufacture and validation of prototypes, ensuring compliance with specifications and scalability for full production runs.
• Identify and implement enhancements to machinery, processes, and methods to improve efficiency and output.
• Lead initiatives to reduce operational costs while improving delivery performance.
• Apply and continually develop lean manufacturing practices throughout the facility.
• Support the introduction and roll-out of a new ERP system, including process development.
• Work collaboratively with the wider engineering department, ensuring adaptability across projects and tasks.
• Maintain accurate technical documentation in line with company policies and engineering standards.
• Suggest and contribute ideas for new product or service developments to enhance customer offerings.

Candidate Profile

• Degree in Manufacturing, Mechanical, Industrial Engineering, or a related discipline.
• Lean Six Sigma training or certification (Green Belt or higher preferred).
• Familiarity with ERP systems; hands-on implementation experience is a plus.
• 2–5 years' experience in a manufacturing or industrial engineering role.
• Background in process development, optimisation, and continuous improvement.
• Exposure to prototype manufacturing, testing, and validation processes.
• Practical experience with lean tools and cost-reduction projects.
• Competence in equipment setup, troubleshooting, and production support.

Technical Competencies

• Strong understanding of manufacturing processes, equipment, and methodologies.
• Skilled in CAD software (SolidWorks, AutoCAD or similar) for process and tooling design.
• Knowledge of quality assurance methods and use of statistical tools for analysis.
• Experience with RCA, FMEA, and CAPA methodologies.
• Awareness of health, safety, and regulatory requirements in manufacturing settings.
• Ability to work effectively with cross-functional teams including production, quality, and supply chain.
• Strong documentation and communication skills.
• Flexible and capable of managing multiple projects simultaneously.
• Proactive mindset with a focus on continuous improvement and innovation.

Our client, a global leader in medical device industry based in Galway, is looking for skilled Quality Engineers / Manufacturing Engineers.

This is an excellent opportunity to work onsite and partner closely with manufacturing and quality teams to strengthen compliance and support process validation projects.

For more info: contact Mark:

or

Responsibilities

• Work alongside manufacturing owners to identify gaps and implement corrective actions to achieve compliance.
• Contribute to equipment and process validation activities (IQ/OQ/PQ).
• Revise and maintain quality system records and technical documentation to ensure audit readiness.
• Lead and support the closure of CAPAs and NCRs with robust corrective actions.
• Develop clear, accurate technical documentation and SOPs for quality and manufacturing processes.
• Collaborate with cross-functional teams, including Manufacturing, Quality, and Regulatory, to deliver sustainable solutions.

Skills & Experience Required

• Degree in Engineering, Quality, or a related discipline.
• 2–5 years of experience in medical device manufacturing, quality engineering, or remediation work.
• Strong background in process validation (IQ/OQ/PQ) and CAPA/NCR resolution.
• Excellent technical writing and documentation abilities.
• Solid understanding of 21 CFR Part 820 and ISO 13485 requirements.
• Strong problem-solving mindset, with the ability to drive issues to fully compliant solutions.
• Willingness to work onsite in Galway.

ICS Medical Devices is currently seeking candidates for the position of Manufacturing Engineer.

ICS is a leading contract design development, prototyping and manufacturing partner serving medical device OEMs in the catheter technology field throughout the world.

The ICS design and manufacturing business has scaled significantly over the last four years with the addition of new projects – ICS is now seeking excellent candidates to support our Manufacturing Engineering group specifically driving process and manufacturing excellence in our manufacturing group.

The candidate will be a strong performer reporting to the manufacturing engineering manager, the succesful candidate will need to

• Support our manufacturing business. Ensure delivery of customer product and expectations.

• Drive manufacturing and process excellence, drive continuous improvement projects to improve yields throughput and overall quality for our customers.

• Support NPI projects and process validation projects as new product transfer to production at ICS.

• Support our production teams with training, process improvements, problem investigation, process updates, documentation updates and customer communication.

As ICS Medical Devices performs to its potential, we rely on our people to meet theirs. If you are the person who wants to learn more and do more, then we encourage you to consider us here in Ballybrit Galway.

Roles & Responsibilities

Customer First

· Technically Lead customer projects in pilot and commercial manufacturing,

· Work closely with assigned teams to deliver projects and production volumes successfully to our customers .

· Customer communication - be technical contact with the customer.

· Deliver customer expectations, customer is our priority.

Execute projects

· Technically – develop technical solutions to improve our processes and manufacturing lines for the customer product.

· Systems – implement and improve procedures, training and workflows per our quality systems.

· Process – develop and install process capable of meeting design specification and process that are capable of manufacturing customer product efficiently.

Team

· Operate in a team environment, operate well with all members of our team.

· Be flexible in support of projects and business goals and priorities.

· Operate in safe, efficient and clean manner.

· Seek opportunities for improvement for self and for the team and for the business.

Quality

· Customer expectations are our focus, always consider quality of output.

· Operated within the ICS Medical Devices quality system.

Self

· Become proficient in our technologies including Catheter Braiding, Coiling and Reflow technologies, laser welding, catheter assembly including thermal bonding, adhesive bond, pad printing, annealing and many more.

· Know our business systems and processes, know our quality systems.

· Learn about product development and the business of medical devices.

· Develop and enhance your project management, communication and customer skills.

· Build your experience and knowledge as you look to drive our business and your career forward.

Requirements

· Degree or equivalent in engineering or equivalent.

· Experiences in catheter assembly technologies a significant advantage.

· Experience in manufacturing, NPI and Process Development an advantage.

· Proven technical capability.

· Strong organizational and communication skills.

· Team player. Flexible, Responsive, an ability to get it done, go the extra mile.

Job Types: Full-time, Permanent

Benefits:

• Bike to work scheme
• Company events
• Company pension
• Employee assistance program
• On-site parking
• Private medical insurance

Education:

• Bachelor's (required)

Experience:

• Medical Device: 1 year (preferred)
• Indsutry: 2 years (required)

Work authorisation:

• Ireland (required)

Work Location: In person

Position:
Manufacturing Engineer

Department:
Engineering

Reporting to:
Group Engineering Lead

Contract type:
Full time Permanent

Summary:

Working within the core Engineering group, as an ME you will play a crucial role in the successful manufacture of our medical devices. You will leverage your technical expertise, problem-solving abilities, and validation experience to ensure the efficiency and quality of our manufacturing processes.

Key Responsibilities:

· To execute tasks as assigned within projects and lead assigned work tasks to successful outcomes.

· To implement appropriate process controls for manufacturing processes for robust and repeatable commercial manufacturing.

· To maximize manufacturing process performance through implementation of continuous improvement methodology.

· To apply a scientific approach to problem solving, combining analytical and experimental skills to maximize efficiency.

· To ensure that all Engineering work and designs are carried out to appropriate GMP, QA/Regulatory Authority standards and Environmental Health and Safety standards.

· To support the development of new processes in conjunction with Automation Engineering ensuring that new processes are stable and capable.

· To provide technical support to new product/ technology introductions and ensure changes are effectively managed.

· To ensure that non-conforming products and processes are evaluated and corrected on assigned responsibilities in accordance with process controls and procedures.

· To successfully complete validations and process improvements using statistical tools and six sigma techniques.

· To support the development of in-house Subject Matter Experts (SME) across the range of core technologies.

· To support process/ equipment/ H&S risk assessment and analysis of risk to product or user.

Qualification Requirements:

· Honors Degree Level 8 in Engineering or equivalent discipline.

· A minimum of 3-5 years of professional experience in a responsible Manufacturing Engineering role within the Medical Device/Healthcare.

Knowledge, Skills and Abilities:

·
Balloon forming experience required. Ability to identify optimal forming parameters for yield and functional performance.

·
Proven and successful implementation of continuous improvement initiatives is essential.

·
Proficiency in CAD software.

· Strong report writing and documentation skills, with high attention to detail.

· Strong knowledge of regulatory requirements and quality standards.

· Knowledge of validation and qualification (IQ, OQ, PQ) for equipment and processes.

Other:

• Responsible for providing regular progress updates to senior management and leading or participating in routine manufacturing meetings to support operational goals.
• Maintain metrics and report weekly on each metric.

Req ID:

Remote Position: No

Region: Europe

Country: Ireland

State/Province: Galway

City: Galway

General Overview

Functional Area:
Engineering

Career Stream:
Process Engineering Manufacturing

SAP Short Name:
ENG-ENG-PRM

Job Level:
Level 07

IC/MGR:
Individual Contributor

Direct/Indirect Indicator:
Indirect

Summary
Great oportunity to join us as Shift Engineer: A Shift: Monday, Tuesday, Wednesday and every second Sunday: 8 AM - 8 PM

Your day-to-day activities will include the following…

• Create, execute, coordinate, and support the design of experiments, test methods, protocols, specifications, and validation documentation (IQ/OQ/PQ) and oversee the development and execution of qualification trials/characterization studies.
• Oversee and analyze the performance of equipment, vision systems and machines, optimizing process parameters to eliminate non-conforming products, low yields, or product quality issues.
• Champion and drive continuous improvement processes for production areas using structured Process Capability and Lean Six Sigma methodologies, leading cross-functional teams in these initiatives.
• Manage multiple projects, generate comprehensive project plans, and support as a team player project teams to drive completion and success, ensuring alignment with strategic objectives.
• Support the maintenance and calibration of critical equipment-systems, ensuring compliance and optimizing maintenance schedules.
• Work with cross-functional teams and external vendors to integrate new products, processes, and technologies into the existing manufacturing area, leading the technology transfer and implementation.

Detailed Description

Performs tasks such as, but not limited to, the following:

• Design, develop, and implement new manufacturing processes to support customer products.
• Develop application software and tooling for a series of complex machines and mechanical process steps within a manufacturing sector.
• Execute with support, capability of machines and process steps using Design of Experiments and statistical methods to ensure maximum utilization of critical resources, maximum throughput, minimum cost and capacity growth; involves integrating equipment, people, material flow, and information systems.
• Solve technical product, process, component, and related problems that affect the efficient operation and/or manufacture of products.
• Provide feedback to product designers on suitability of designs for manufacturability with supervision.

Knowledge/Skills/Competencies

What do we expect from you?

• Experience using engineering tools and software packages to support automated manufacturing processes.
• Proven experience in detailed analysis, modelling, and methodologies to validate manufacturing process and tooling design and specifications.
• Experience in creating SOP's, Control Plans, and performing validation (FAT, SAT, IQ, OQ, PQ).
• Demonstrated ability to effectively communicate manufacturing plans, proposals, and results, and negotiate options at executive management levels.
• Experience in analytical and problem-solving skills.
• Excellent interpersonal and communication skills.
• A strong aptitude for report writing and data analytics.
• An advantage with knowledge of the medical device industry and of 21 CFR, (820, 11), ISO13485, specifically in the areas of Change Control and Validation.

What are we looking for?

• A minimum of 4+ years' experience in a Process Engineering role, with a proven track record of involvement in projects and teams.
• A Primary Degree in an Engineering/Science discipline.
• Medical Device AND/OR Automation experience an advantage.
• Experience in a highly automated manufacturing environment.
• An ability to initiate and lead change, collaborate and create alignment, drive accountability, think critically, and make sound decisions.

What do we ofer?

• Market-competitive total reward: flexible salary, fix and variable salary based on goals
• The opportunity to work with new product introduction teams in the Health Tech sector.
• Engineering Function driven by innovation where creativity matters.
• Training and development opportunities; with us, the sky is the limit
• The opportunity to innovate, learn, mentor others, and work toward your own vision of career success
• A global, collaborative culture with strong leadership imperatives to foster your growth and professional opportunities
• A sustainable culture where we provide opportunities for employees to give back to the community

Notes

This job description is not intended to be an exhaustive list of all duties and responsibilities of the position. Employees are held accountable for all duties of the job. Job duties and the % of time identified for any function are subject to change at any time.

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.

Company Overview
Celestica (NYSE, TSX: CLS) enables the world's best brands. Through our recognized customer-centric approach, we partner with leading companies in Aerospace and Defense, Communications, Enterprise, HealthTech, Industrial, Capital Equipment and Energy to deliver solutions for their most complex challenges. As a leader in design, manufacturing, hardware platform and supply chain solutions, Celestica brings global expertise and insight at every stage of product development – from drawing board to full-scale production and after-market services for products from advanced medical devices, to highly engineered aviation systems, to next-generation hardware platform solutions for the Cloud. Headquartered in Toronto, with talented teams spanning 40+ locations in 13 countries across the Americas, Europe and Asia, we imagine, develop and deliver a better future with our customers.

Celestica would like to thank all applicants, however, only qualified applicants will be contacted.

Celestica does not accept unsolicited resumes from recruitment agencies or fee based recruitment services.

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%

We are recruiting a Manufacturing & Quality Engineer for our clients in County Cork. The role focuses on improving manufacturing processes, ensuring high-quality production standards, and supporting product innovation. The successful candidate will work closely with production, R&D, and quality teams to deliver consistent, efficient, and reliable manufacturing operations. This is a full time, permanent position based within easy commute of both Killarney and Macroom.

Key Responsibilities

• Monitor and improve manufacturing processes to enhance efficiency, safety, and product quality.
• Develop, implement, and maintain quality control procedures and standards across production lines.
• Conduct root cause analysis for production and quality issues and implement corrective actions.
• Support new product introductions, ensuring manufacturability and quality compliance.
• Collaborate with R&D and engineering teams to optimize production processes.
• Perform audits, inspections, and testing to ensure compliance with internal and regulatory standards.
• Maintain accurate documentation for quality records, production reports, and continuous improvement initiatives.
• Provide training and guidance to production staff on quality procedures and best practices.

Key Requirements

• Degree or Diploma in Mechanical, Manufacturing, Industrial, or Quality Engineering.
• Minimum 2–3 years' experience in manufacturing or quality engineering, preferably in the HVAC, appliance, or FMCG sectors.
• Strong knowledge of lean manufacturing, Six Sigma, and continuous improvement methodologies.
• Familiarity with quality standards such as ISO 9001 and regulatory compliance.
• Excellent problem-solving, analytical, and communication skills.
• Proficient in ERP systems, Microsoft Office, and data analysis tools.

Salary is open to negotiation, based on experiences. For further information, please email me directly