577 Development 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.

At Freudenberg Medical, we make products that save and improve the lives of people every day, all around the world. We are a global provider for medical device design and manufacturing with more than 2,500 employees. Innovation is at the core of our company, and we are proud of our industry-leading quality, lean manufacturing, and focus on innovation in products and processing technologies. Freudenberg Medical is an exciting place to work with lots of opportunity to learn, develop, and grow your career. Come join us and together we can make a difference in the future of healthcare.

Some of your Benefits
Company Pension:
Save for retirement with the company's help.

Health Insurance:
Rely on comprehensive services whenever you need it.

Flexible Work Models:
We allow for flexible work models to ensure both professional and personal success.

International Opportunities:
Grow in your career through international exchange and global job opportunities.

Diversity & Inclusion:
We focus on providing an inclusive environment and recognize our diversity contributes to our success.

Carrick-on-Shannon, Co. Leitrim

Hybrid Work

VistaMed Ltd.

You support our team as

Research & Development Engineer
Responsibilities

• Create product and tooling drawings to support quotes, prototyping, and process development
• Develop and present product and process concepts, including prototypes
• Provide technical support to Sales and Marketing and assist in creating quotations
• Respond to customer enquiries with clear written and verbal communication
• Design and develop new products, materials, equipment, and processes from concept to design freeze
• Manage projects to meet timelines, cost targets, and technical deliverables
• Ensure full compliance with Quality, Regulatory, Health & Safety, and documentation requirements
• Transfer new products to manufacturing and support validations and staff training
• Drive continuous improvement using Lean tools (3P, 5S, DMAIC, Six Sigma)
• Mentor and support junior engineers and technical staff
• Collaborate with Production, Quality, and Technical teams as needed
• Support activities such as CAPAs, audits, and validations
• Ensure health, safety, environmental, and energy standards (ISO 45001, 14001, are integrated into design and development

Qualifications

• Bachelor's degree in Engineering or Science (Mechanical, Biomedical, Manufacturing, Automation, or related field)
• Experience with CAD systems (ideally Solid Edge)
• 2–3 years' experience in the medical device industry preferred
• Knowledge of extrusion-based catheter assemblies is an advantage
• Strong communication and interpersonal skills
• Self-motivated with the ability to manage multiple tasks in a fast-paced environment
• Proficient in Microsoft Office (Excel, PowerPoint, Word)
• Junior/Associate roles available for candidates with limited experience - support and co-signing provided

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.

The primary responsibility of this position is to support / lead on the design, development and taking to market of medical devices for Cook Medical.

Reporting to: Team Lead, Research and Development / Manager, Research and Development

Find out more about Cook Medical here

Responsibilities

• Perform Duties of Research & Development Engineer 2:

• Design development, prototyping, test method design, design evaluation , design reviews, design specifications, design verification and validation, design protocols and reports, transfer to production activities in a timely effective manner.

• Product testing and evaluation, completion of test reports to support design selection.
• Preparation and presentation of design reviews.
• Product risk analysis and risk management.
• Contribute towards process development during introduction /development of new equipment and production processes as required for any new manufacturing techniques.
• Source new materials components and equipment.
• Development of component specifications, inspection methods, bills of materials and manufacturing processes.

• Introduction of new equipment, materials and technologies.

• As required work closely with Key Opinion Leaders, physicians, product managers and team to develop innovative medical devices to improve patient care.

• Work closely with Project Lead and take responsibility for assigned research and development project tasks:

• Manage and drive assigned project tasks to ensure timely completion of project milestones.

• Work closely with cross functional groups to achieve project and company goals.
• Product performance evaluations.
• Contribute to innovation and creativity within team through filing of disclosures and patents.
• Hold regular project meetings and document minutes and actions.

• Ensure project milestones are achieved to meet business metrics.

• Communications:

• Regular communication to cross-functional teams and senior management.

• Project status communications and reporting.

• Remain on the forefront of emerging industry practices.

• Educating oneself in the medical area for which the new devices are being developed in order to have an appreciation for what needs to be achieved with these products.
• Support other cross functional groups to deliver company goals.
• Ensure that Cook's Code of Conduct is considered in all business matters carried out on Cook's behalf.

Qualifications

• Bachelor's degree is required, preferably in engineering or a related field.
• Minimum of 3 years' relevant experience is desired.
• Project planning/execution skills.
• Execution of project in a timely effective manner.
• Knowledge of anatomy and physiology.
• Good mechanical design and understanding of engineering fundamentals with medical device materials knowledge.
• Statistical understanding and experience.
• Manufacturing design and process understanding.
• Good working knowledge of Solidworks and/or Pro Engineer CAD.
• Strong technical writer.
• Knowledge of relevant ISO, EU, FDA medical device standards regulations is required.
• Willingness and availability to travel on company business.

About the Opportunity

Join a leading medical device company in Galway, Ireland, as an R&D Engineer II. Use your mechanical engineering and CAD skills to design innovative medical devices in a dynamic, collaborative environment.

Key Responsibilities

• Develop device concepts to meet performance goals.
• Build and test prototypes; analyse data for solutions.
• Create drawings using SolidWorks.
• Select materials and assembly methods.
• Collaborate with cross-functional teams for system integration.
• Work with vendors to meet project goals.
• Write protocols and reports; document designs.
• Ensure ISO 13485 and QMS compliance.

Qualifications & Experience

• Honours degree in Mechanical or Biomedical Engineering or equivalent.
• 3+ years in medical device design, prototyping, and testing.
• Proficient in SolidWorks (Autodesk Fusion a plus).
• Knowledge of ISO 13485 and QMS.
• Experience in material selection and design validation.

Skills & Behaviours

• Strong mechanical engineering and design skills.
• Excellent problem-solving and initiative.
• Strong communication and presentation skills.
• Team player with multitasking ability.
• Interest in industry trends and technologies.

Research & Development Engineer (Vascular)

We are actively seeking to recruit a Research and Development Engineer to become a key member of the R&D Team within a leading Limerick based Medical Device multinational.

This is an excellent opportunity to advance your career within a fast paced dynamic environment.

Responsibilities:

• Design development, prototyping, test method design, design evaluation, design reviews, design specifications, design verification and validation, design protocols and reports, transfer to production activities in a timely effective manner.
• Product testing and evaluation, completion of test reports to support design selection.
• Preparation and presentation of design reviews.
• Product and project risk analysis and risk management.
• Development of the Design History File
• Work with Process Development Engineering to introduce/develop new equipment and production processes as required for any new manufacturing techniques.
• Source new materials components and equipment.
• Development of component specifications, inspection methods, bills of materials and manufacturing processes.
• Introduction of new equipment, materials and technologies.
• Work closely with Key Opinion Leaders (KOL's), physicians and product managers to develop innovative medical devices to improve patient care.
• Project lead for assigned research & development projects including technical and project management responsibly.

Qualifications and Experience:

• Third level degree in Mechanical, Biomedical, Science, Design or similar discipline.
• 3+ years' design experience in medical device roles.
• Third level degree in Mechanical, Biomedical, Science, Design or similar discipline.
• Project planning skills.
• Execution of project in a timely effective manner.
• Knowledge of anatomy and physiology.
• Good mechanical design and understanding of engineering fundamentals with extensive medical device materials knowledge.
• Manufacturing design and process understanding.
• Good working knowledge of Solidworks and/or Pro Engineer CAD.
• Strong technical writer.
• Knowledge of medical device quality & regulatory systems and medical device directives (ISO13485 and FDA CFR 820), EU Medical Device Regulation 2017/745.
• Team Player with ability to develop strong working relationships.
• Strong communication and inter-personal skills.
• Good problem solving skills.
• Highly motivated individual, self-starter with a passion for excellence.
• Must be able to work in a fast paced environment.
• Willingness and availability to travel on company business.

R&D Engineer - Design Control, 12-month contract role

• 12-months contract (with intention to extend)
• Flexible day rate (DOE)
• Globally recognised company

This company is looking for an
R&D Engineer
to join their dynamic endoscopy team. In this role, you will work as part of the end-to-end developement team to design products that positively impact patients lives globally.

Diligent documentation of design changes history and regulatory compliance will be the primary focus of this poisiton within the team.

This role is a fantastic long-term opportunitiy to build your career in a thirving, industry leading pharmaceutical company.

What You'll Do:

• Support end-to-end design and development of advanced medical devices in the endoscopy space
• Properly document continuous improvement initiatives in product design and development in accordance with regulatory and best practise guidelines.

What We're Looking For:

• 3-5+ years' experience in the medical device industry, preferably in R&D.
• Strong understanding of
  design controls, risk management, and regulatory compliance
  .
• Proven ability to adopt new
  RMS, ALM and design control systems

Pay rate:

€ per day (Flexible depending on experience)

Contract Length

12-months (rolling thereafter)

For more information contact Joseph Sweeney by emailing your CV to

Planet Pharma is seeking a vascular R&D Engineer working on a transformative Class III implantable device for aortic endovascular repair. This high-impact program which will progress through clinical studies, PMA submission, and global commercialization. You'll lead the delivery system workstream, one of three core components of the device (alongside stent and graft covering), and manage a dedicated sub-team within a broader cross-functional group.

Key Responsibilities

• Lead the design and development of the
  delivery system
  for an aortic stent graft, from concept through to commercialization
• Manage and mentor a team of engineers.
• Drive structured project execution across design, verification, validation, and regulatory milestones
• Collaborate with clinical, regulatory, and manufacturing teams to ensure alignment with FDA Class III device requirements and PMA strategy
• Support clinical trial preparation and execution, including design transfer and documentation
• Ensure robust design control, risk management, and compliance with ISO 13485 and FDA 21 CFR Part 820
• Foster innovation and technical excellence while maintaining a disciplined, milestone-driven approach

Required Qualifications

• Bachelor's or Master's degree in
  Biomedical Engineering
  ,
  Mechanical Engineering
  , or
  Materials Science
• Minimum
  5 years' experience
  in medical device engineering, specifically Class III implantable devices
• Proven expertise in
  vascular technologies
  , ideally with
  aortic stent grafts
  , or alternatively in
  coronary stents/stent grafts
• Demonstrated
  leadership experience
  , with ability to delegate, motivate, and guide teams through full product lifecycle
• Strong organizational skills and a structured approach to problem-solving and project management

What You'll Gain

• A chance to shape a next-generation vascular device with global impact
• Exposure to clinical and regulatory strategy for PMA and international markets
• A collaborative, mission-driven culture focused on improving patient outcomes

Research and Development Engineer (Contract)

Location:
Galway, Ireland

Contract Type:
Contractor (Onsite or Hybrid – as required)

Role Overview:

A leading global organisation in the healthcare technology sector is currently seeking a
Research and Development Engineer (Contractor)
to support a
Shelf-Life Extension project
for a range of commercial medical products. This role is ideally suited to someone with a strong background in
Design Control
,
Design Verification
, and
technical documentation
, along with a solid understanding of
material science
,
product testing
, and
regulatory standards.

Key Responsibilities:

• Contribute to the planning and execution of shelf-life extension strategies for existing medical products, ensuring alignment with quality and regulatory requirements.
• Develop and carry out Design Verification activities, including writing and executing protocols and compiling detailed reports.
• Analyse and interpret the impact of material ageing on product performance and safety.
• Determine appropriate sample sizes and selection criteria, applying sound statistical methods (including variable and attribute data analysis).
• Work extensively with technical documentation, including Bills of Materials (BOMs), Process Plans, design drawings, and specifications.
• Support regulatory submissions and design documentation updates in line with project changes.
• Collaborate with cross-functional teams to drive project deliverables and escalate technical challenges when necessary.
• Maintain a proactive and solutions-oriented approach to technical problem-solving.

Qualifications and Experience:

• Degree in Engineering or a related technical field (Level 8 or higher); postgraduate qualification is an advantage.
• Experience in a regulated environment, preferably medical devices or a similarly structured industry.
• Strong working knowledge of
  Design Control processes
  , particularly in the context of product lifecycle extension.
• Proven track record with
  Design Verification
  —from protocol creation to report generation.
• Excellent technical writing and documentation skills.
• Familiarity with
  material properties
  ,
  ageing studies
  , and related testing methodologies.
• Understanding of
  product specifications
  ,
  test method validation
  , and statistical approaches to sample testing.
• Comfortable navigating complex technical documents such as BOMs, drawings, and process documentation.
• Working knowledge of
  risk management processes
  and
  regulatory standards
  (e.g., ISO 13485, FDA QSR).
• Ability to work independently while also contributing effectively within a multidisciplinary team environment.

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients— that is what Vantive aspires to deliver.

We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don't settle for the mediocre. Each of us is driven to help improve patients' lives worldwide. Join us in advancing our mission to extend lives and expand possibilities.

A CV must be attached to your application.

In our Product Development department you will be responsible for management of product specific projects. You will coordinate new R&D led projects including New Product Introduction (NPI) in the manufacturing plant. You will be involved in face-to-face meetings, teleconferences and regular updates on project activities, milestones and status.

Essential Duties and Responsibilities:

The Product Development Engineer will have responsibility for management of product specific projects including:

• Coordinating new R&D led projects including New Product Introduction (NPI) in the manufacturing plant including face-to-face meetings, teleconferences and regular updates on project activities, milestones and status.
• Writing validation protocols for trials, coordinating and executing trials and writing protocol trial reports.
• Responsibility for project administration and compliance to project plans.
• Managing product, process and supplier changes which have a potential impact on products manufactured in Castlebar.
• Coordination and assistance with Project EMS boards
• Coordination of projects that are Value Improvement Processes (VIPs) for the plant.
• Analytical thinking using established tools for trouble shooting and investigation management.
• Help develop best practices to for product development procedures.

Education and experience requirements:

• Degree in Science (Engineering, Chemistry, Biology).
• Strong relevant Pharmaceutical/Healthcare experience.
• Proven ability to work cross functionally as this role requires interaction with different functions within the plant.
• Ability to communicate (written and verbal) in a clear and concise manner.

What can Vantive offer to you:

• A stable and secure work environment
• A comprehensive benefits package, including private medical insurance, company pension scheme, and annual bonus scheme
• A collaborative and dynamic work environment
• Access to state-of-the-art equipment and technology
• Recognition and reward for outstanding performance

Reasonable Accommodation

Vantive is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Form Link

Recruitment Fraud Notice

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Position Summary

This position is responsible for meeting the goals and objectives of the organization by supporting the efficient and innovative development of products that meet customer needs, align with market trends, and contribute to profitable growth.

Essential Duties and Tasks

To perform this job successfully, an individual must be able to perform each essential job function satisfactorily. Reasonable accommodations may be made, upon request, to enable individuals with disabilities to perform the essential functions.

· Assist in the development and execution of both strategic and customer-specific projects by identifying customer requirements, defining materials, structures, and converting processes, and supporting next-generation innovations.

· Collaborate with R&D, operations, quality, supply chain, and commercial teams to ensure alignment, timely execution, and successful commercialization of new and modified products.

· Plan, write, and execute product trials at manufacturing plants and customer facilities; gather and interpret results to ensure commercial specifications and quality standards are met.

· Offer technical support in material selection, converting processes, and product construction; contribute to defining and updating bills of materials and cost estimates for new and existing products.

· Demonstrate ongoing commitment to ISO standards, Good Manufacturing Practices (GMPs), and food safety procedures in all aspects of product development.

· Prepare detailed trial reports, presentations, and project updates for internal teams and customers; document testing outcomes and process changes accurately.

· Assist in estimating the cost and timeline for development projects by analyzing materials, processes, and labor inputs.

· Define testing protocols and interpret statistical data to validate performance, ensure compliance with customer specifications, and drive improvements.

· Track performance of new and modified products post-launch; recommend enhancements based on data, customer feedback, and manufacturing insights.

· Demonstrate a positive and professional attitude in all interactions with coworkers, customers, and suppliers, promoting a collaborative and respectful working environment.

· All other duties as assigned.

Qualifications, Education and Experience

· Associate's Degree in a related field or equivalent experience. required; Bachelor's Degree in a related field or equivalent experience. preferred

· 2-4 years' experience in a related field experience in a related field required.

· Experience using Microsoft Office Suite (Word, Excel, PowerPoint), Visio, Outlook Email, and calendar.

· Maintains strict confidentiality and protects privacy of confidential/sensitive information.

· Exceptional time management and organization skills. Ability to manage multiple tasks and projects simultaneously establishing priorities to meet deadlines.

· Ability to communicate effectively (verbal, written, and presentations) with executive leadership, staff, and internal and external clients.

· Proactive; exercises sound judgment and decision-making; able to identify problems and needs and develop solutions and/or options.

· Self-confident, self-motivated polished professional who thrives in a challenging, fast-paced environment

Job Type: Full-time

Benefits:

• Bike to work scheme
• Company events
• Employee assistance program
• On-site parking
• Wellness program

Work Location: In person