What Jobs are available for Research And Development Engineer 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.

Senior Engineer, Research and Development

About the Company

Join a global leader in diabetes care dedicated to empowering people to live healthier, fuller lives through innovative medical technologies. With a strong focus on collaboration, inclusion, and continuous learning, this organization offers a dynamic environment where your ideas and expertise truly make an impact.

About the Position

This is an exciting opportunity for an experienced Senior R&D Engineer to lead complex engineering initiatives and drive innovation in product and technology development. You'll play a key role in advancing life-changing solutions, mentoring technical talent, and shaping the future of diabetes care.

Key Responsibilities

• Lead the design and development of novel medical technologies aligned with the company's strategic goals.
• Manage R&D projects from concept to completion, ensuring quality, safety, and compliance standards are met.
• Collaborate cross-functionally to solve advanced technical challenges and deliver impactful solutions.
• Mentor and guide engineers, fostering a culture of innovation and continuous improvement.
• Drive process efficiencies, manage budgets, and represent R&D in key meetings and external engagements.

Experience/Requirements

• Bachelor's degree in Mechanical or Biomedical Engineering (Master's preferred).
• 10+ years' experience in product development, including at least 5 years in medical devices.
• Proven leadership in complex R&D programs with strong problem-solving and project management skills.
• Excellent communication, collaboration, and analytical thinking abilities.
• Passion for innovation, inclusion, and delivering meaningful healthcare solutions.

Remuneration Package

Salary of €110,000

Healthcare

Pension scheme of up to 9.75%

24 days holidays

Plus more

Job title:
Senior R&D Engineer

Location:
Ballybrit, Galway

Benefits:
Excellent salary, bonus, pension, healthcare and opportunity to grow your career with hugely exciting Medical Device organisation.

Company:

My client are a Medical Device company who have recently been acquired by a multinational, a global leader in neurovascular care. And a broad portfolio of devices used in the endovascular treatment of haemorrhagic and ischemic stroke.

About the role:

As a Senior R&D Engineer you will work on a brand new product from concept to commercialisation. Also supporting and delivering complex acute ischemic stroke projects with significant technical challenges. Overall responsibility for various aspects of new development projects.

Some responsibilities include:

• Develop an understanding of the disease state, gather user needs, and translate into technical specifications.
• Support the management of the direct team to deliver on performance, time and cost targets.
• Generate creative product solutions to address unmet needs.
• Develop test models for prototype performance evaluations.
• Build and test prototypes; analyse test data and interpret to identify optimal solution(s).
• Create detailed component and finished device assembly drawings/specifications.
• Identify and select product materials, assembly methods and define process settings.
• Identify and manage of key risks throughout the product lifecycle.
• Evaluate and assess physician (user) techniques and develop product training materials.

Requirements:

• A minimum of 5 years' experience in all stages of medical device design and development (including design with SolidWorks, prototyping, and testing) is required.
• Mechanical or biomedical engineering degree or equivalent.
• Specific experience on Medical Devices, cardiovascular or neurovascular implants or instruments including catheters, stents, delivery systems.
• Strong design and technical ability based on a broad and deep knowledge of fundamental engineering principles.

What awaits you:

This is an opportunity to work with a ground-breaking biomedical operation, part of a company with an excellent record in employee continuous professional development and business improvement.

• An opportunity to be part of a global market leader.
• A dynamic and inspiring working environment.
• Opportunities to work on challenging projects and assignments.
• Possibilities for further personal and professional development/education.
• Excellent benefits

Does this sound like your next career move? To apply and For more info forward your application to the link provided or contact me on OR