400 Manufacturing Trainee 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

Barden is proud to partner exclusively with a leading FMCG company to find a talented
qualified accountant
ready to take the next step in their career. This is a fantastic opportunity to join a dynamic manufacturing site and play a key role in driving performance and strategic decision-making.

What You'll Be Doing:

• Act as a
  business partner
  across finance and non-finance teams
• Lead performance tracking through
  balanced scorecards
  and KPIs
• Own the
  budgeting and forecasting
  process
• Present insights and updates to
  senior stakeholders and shareholders
• Identify and implement
  process improvements
• Dive into
  financial analysis
  and support on
  ad-hoc strategic projects

Who We're Looking For:

• CIMA or ACCA qualified
  accountant
• 1–4 years'
  post-qualification experience
  in industry
• Manufacturing/FMCG experience is essential
• Solid grounding in
  cost or management accounting
• Strong
  analytical mindset
  and attention to detail
• Excellent
  communication skills
  and confidence engaging across all level

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.

Job Description

Summary:

Site lead for Contract Manufacturing Organizations (CMOs).

Single point of accountability and interface between Amgen and assigned external partners.

Responsibilities:

Manufacturing operations: Develop and lead robust business processes, maintain reliable relationships with contract site management; assess industry trends, internal network, and technology advancements as tools to improve contract site performance. Manage budget development, monitoring, and reporting; create and manage contracts - confidentiality disclosure agreement(s), scope of work agreement(s), request for pricing/information, supply agreement(s) etc.; monitor and improve financials with CMO; actively manage and communicate forecasts to the sites and manage capacity planning. Drive operational excellence and champion change.

Site performance monitoring: Manage contract site performance using lean tools and PDCA, lead site operating review meetings; drive improvements at contract sites; sustain and improve the overall health of the business, and lead communication/relationship with the contract site as well as internal management.

Project Management and Technology transfer: Lead a department-wide project from conception to implementation and close-out. Present to and obtain buy-in for value proposition of such projects to senior management. Provide oversight of all planning and coordination of product transfer activities to the contract site(s); develop, present, and obtain approval of budget, timeline and ensure execution of transfer team activities to achieve seamless product transfer to the contract site(s); ensure risk management initiatives are taking place as per RM plan; lead site issue management and resolution; provide issue escalation to executive management.

Qualifications:

Minimum requirements (as per standard)

Preferred Requirements:

• Bachelor's in Business Administration, Engineering, or Science-related field
• 5+ years of experience in protein, API, DS, DP, or packaging manufacturing environment
• 5+ years in roles requiring knowledge of cGMP principles, FDA and other regulatory guidelines, and validation principles
• 2+ years of experience working with external parties and/or leading cross-functional teams for clinical and/or commercial products
• 1+ years of project management experience leading multi-functional and multi-location team
• 1+ years of experience across ACM or CMQ
• Ability to travel +/- 20% of time (domestic and international)

Competencies:

• Demonstrated competencies of lower GCF levels.
• Demonstrated matrix management and influencing skills.
• Manufacturing and cGMP knowledge / experience.
• Demonstrated negotiation skills.
• Operational Excellence proficiency and ability to drive continuous improvement.
• Financial/budgeting knowledge and business acumen.
• Proficient project management skills.
• Problem-solving and critical thinking.
• Understanding of contractual requirements.
• Technical writing and multi-level communication skills.
• Demonstrated ability to lead effectively in collaborative/team environment.
• Demonstrated ability to take initiative, drive action, and work under minimum supervision.

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

Manufacturing Manager

ABOUT THE COMPANY

An innovative medical technology start-up with operations in Ireland is developing next-generation imaging solutions that aim to transform healthcare and address significant global clinical challenges. With a strong focus on engineering excellence, creativity, and collaboration, the company is building advanced hardware, software, and data science technologies that push the boundaries of medical imaging.

To support continued growth, the team is seeking an experienced
Manufacturing Manager
to lead manufacturing activities and oversee partnerships with key manufacturing partners across Ireland and mainland Europe. This position will require regular on-site engagement with these partners.

THE ROLE

The Manufacturing Manager will be responsible for developing, implementing, and maintaining best-in-class manufacturing processes in collaboration with internal teams and contract manufacturers. The successful candidate will establish robust process controls, support design transfer, and scale production from prototype to volume manufacturing, ensuring all operations align with business objectives, quality standards, and regulatory requirements.

This is a hands-on leadership role in a dynamic start-up environment, offering the opportunity to shape the future of medical imaging technology.

KEY RESPONSIBILITIES

• Develop and manage efficient manufacturing processes, including materials planning, production scheduling, and product release for use.
• Partner with R&D on new product development, focusing on Design-for-Manufacturing (DFM) and seamless design transfer to internal or external manufacturing operations.
• Build and maintain strong relationships with third-party manufacturing partners.
• Travel regularly to company and partner manufacturing sites across Ireland and Europe.
• Lead reviews of manufacturing progress, challenges, and production analysis, driving alignment across project and functional teams.
• Maintain manufacturing documentation, including Device Master Records (DMR) and Device History Records (DHR).
• Ensure compliance with Quality Policy and applicable quality system requirements.
• Create and manage the annual manufacturing budget, including cost and capacity modeling.
• Lead continuous improvement initiatives to enhance efficiency, reduce costs, and scale production.
• Promote a collaborative, high-performance culture within the manufacturing function.

EXPERIENCE & QUALIFICATIONS

• Bachelor's degree in Engineering or related discipline with a minimum of 10 years' experience, including at least 5 years in a leadership role within a regulated industry.
• Proven experience working under ISO 13485 and/or FDA-regulated quality systems, with a strong understanding of risk management methodologies.
• Skilled in Design-for-Manufacturing (DFM), Lean manufacturing, and Six Sigma techniques.
• Experience managing global, cross-functional teams and manufacturing partners.
• Experience with sterile disposable medical devices (e.g., intravascular catheters) and/or complex hardware systems is advantageous.
• Demonstrated ability to manage budgets, drive cost improvements, and scale production operations.
• Excellent communication, organizational, and leadership skills.
• Previous start-up experience is a plus.
• Flexible, proactive problem-solver with a collaborative mindset.

WHAT'S ON OFFER

• Opportunity to work on cutting-edge medical imaging technologies that directly improve patient care.
• A dynamic, international team culture focused on innovation, collaboration, and professional growth.
• A flexible, learning-driven work environment with opportunities to expand your technical and leadership skills.
• Offices in Ireland and Germany, with flexible working arrangements and international exposure.

Manufacturing Technician

Reporting Structure

This person shall report to the Senior Manufacturing Engineer or designate.

Overall Job Objectives

The Manufacturing Technician supports day-to-day production by maintaining efficient and compliant operations on the manufacturing line. Key responsibilities include troubleshooting issues, performing equipment setups and maintenance, supporting process improvements, and ensuring accurate documentation in line with GMP and quality standards.

The Manufacturing Technician will work as part of a team to assist in the manufacture of innovative medical devices in accordance with the requirements of International Standards: ISO 13485, FDA 21 CFR Part 820, EU Medical Device Regulation (MDR) and the Vivasure Medical Quality Management System.

Main Duties and Responsibilities

• Provide day-to-day technical support to the manufacturing line to ensure consistent and efficient operations.
• Respond promptly and effectively to manufacturing line stoppages or anomalies to minimise production downtime.
• Troubleshoot and resolve issues related to equipment, tooling, process, or material.
• Perform manufacturing line set-ups and operate equipment, ensuring proper use and functionality.
• Carry out routine and preventative maintenance on production equipment.
• Identify and implement improvements to manufacturing processes, tools, jigs, and methods that enhance product quality, efficiency, and manufacturability.
• Support the elimination of waste and inefficiencies using Lean, Six Sigma, or other continuous improvement methodologies.
• Participate in process development activities for new and existing products.
• Assist with equipment, process and product verification and validation testing.
• Maintain accurate and complete batch records, logs, check sheets, and maintenance records in compliance with GMP and quality system requirements.
• Conduct or support in-process inspection, functional testing, and non-conformance investigations.
• Maintain technical documentation in accordance with Quality Management System requirements.
• Provide input for risk assessments, FMEAs (Failure Modes and Effects Analysis).
• Collaborate with cross-functional teams during line validations, engineering builds or product transfers. Support product builder training on processes & work instructions.
• Work as part of the core manufacturing team to support root cause analysis and implement corrective and preventive actions.
• Maintain equipment, work areas and facilities to ensure a clean and safe work environment and compliance to good manufacturing practice.

Qualification Required

• Third level qualification in a relevant technical field is advantageous.
• Knowledge of quality standards including ISO 13485, MDR, and FDA Requirements.

Work Experience or Training Required

• 2-5 years hands-on experience in
• Medical device / pharma industry
• Operating and maintaining production equipment
• Supporting process improvements
• Working knowledge of QMS and regulatory requirements in the medical device industry.

Special Skills Required

• Excellent communication and organisational skills
• Works effectively in a team environment
• Takes ownership of responsibilities and can work autonomously as required
• Good documentation practices (GDP) and strong working knowledge of Microsoft Word, Excel, Powerpoint etc.
• Knowledge of cleanroom manufacturing processes and methodologies
• Ability to read technical drawings, process diagrams, and equipment manuals.

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.