Veryan has developed innovative technology to improve the performance of vascular stents by adopting the principle of biomimicry; developing structures that imitate those occurring naturally. Veryan’s vascular biomimetic stent technology involves adapting a straight stent design to a three-dimensional helical shape, which more closely mimics the natural geometry of the human vascular system. The BioMimics 3D stent belongs to a new generation of self-expanding stent design with advanced biomechanical and flow performance properties, creating the potential to transform the treatment of patients with symptomatic peripheral arterial disease of the lower limbs. This highly differentiated technology has been clinically proven in a multicentre, randomised clinical trial (the Mimics study) in superficial femoral and proximal popliteal (femoropopliteral) arteries of the leg and received CE Mark approval in November 2012.

Veryan was formed in 2003 as the result of a technology spin out from Imperial College, London, UK. Veryan has designed, patented and developed a highly innovative three dimensional (3D) Nitinol (nickel-titanium alloy) stent technology – BioMimics 3D – based on the pioneering work by Professor Colin Caro (Emeritus Professor of Physiological Mechanics, Dept. of Bioengineering, Imperial College London) on the link between vessel geometry, blood flow mechanics and vascular disease.1

Veryan benefits from a highly experienced Board of Directors and the Company’s management team has built an outstanding development group, supported by a world class Scientific Advisory Board. The Company’s head office is in Horsham, West Sussex, UK, and the research and development facility is in Galway, Ireland.

Science & Healthcare

Veryan Medical

Manufacturing & Electronics

You need a degree in Engineering or a scientific field, 1+ year R&D experience in medical devices, strong biomechanics knowledge, and excellent communication skills.

You will design, develop, and test projects, ensure compliance with regulations, analyze data, support manufacturing processes, and coordinate documentation and protocols.

Research & Development

Engineering

Galway

<div>
 R&amp;D Engineer Full time - Permanent Galway- Hybrid
 We have an exciting opportunity for a R&amp;D Engineer to join Veryan Medical!
 Summary Veryan Medical is a fast-paced, rapidly growing medical device company offering a highly differentiated solution in SFA interventions. We share a commitment, a passion, and a vision for the contribution Veryan makes to innovation in interventional medicine.
 Our team powers Veryan’s business. Whether sales representatives, design engineers, quality engineers, or clinical study managers, our people bring an unmatched expertise in each of their fields that both inspires and challenges.
 Veryan’s culture of innovation helps each individual develop both professionally and personally, and our culture of respect means that we all work in a collaborative, empowering, and exciting environment. We are committed to excellence through our patient-centric approach, and we pride ourselves in our integrity of doing what is right and doing what we say.
 The R&amp;D Engineer will play a key role in Veryan’s current projects and R&amp;D team. This is a great opportunity which will allow the successful candidate to take the next step in their career while working as part of a supportive, collaborative team in the new state-of-the-art facility in Galway.
 
 Job Requirements Principal Responsibilities 
 <ul>
 <li>Perform project tasks ensuring adherence to the company’s procedures which have been developed in compliance with ISO13485, the Medical Device Directives and FDA 21 CFR 820</li>
 <li>To provide design, development and technical input to the Company’s development projects.</li>
 <li>Packaging development, including design and testing required for new and existing products under development.</li>
 <li>Test method Development, document, training, and validation.</li>
 <li>Support the development of manufacturing processes using tools such as design for six sigma (DFSS) and design for manufacturing (DFM).</li>
 <li>Summarise in vitro test data and communicate the results to project teams leaders and functional groups. Demonstrate a working knowledge of concepts &amp; applications in mechanical and process engineering.</li>
 <li>Using the principles of systematic problem solving, learn and execute analytical techniques such as DOE, Six sigma and statistics.</li>
 <li>Work with the QA Department in developing test, verification and validation (including design review) procedures.</li>
 <li>Manage and co-ordinate procedures, protocols, reports and purchases relevant to the R&amp;D tasks assigned to you, keeping the R&amp;D Project Manager updated.</li>
 </ul>
 <ul>
 <li>Other duties as required by the Company.</li>
 </ul> 
 
 Education &amp; Training
 <ul>
 <li>Bachelor’s/Master’s degree in Engineering or local equivalent in a scientific discipline and/or appropriate experience.</li>
 <li>Good communication and interpersonal skills.</li>
 <li>Ability to prioritise project tasks and meet deadlines.</li>
 </ul> 
 
 Experience &amp; Skills
 <ul>
 <li>Minimum of one year experience working as an R&amp;D Engineer in the medical device industry.</li>
 <li>Good knowledge of biomechanics and mechanical analysis &amp; design.</li>
 <li>Strong communication skills both written and verbal.</li>
 </ul> 
 
 Benefits of Working with Veryan:
 <ul>
 <li>Competitive salary and bonus.</li>
 <li>Pension scheme with generous employer contributions.</li>
 <li>Private medical insurance for you, spouse / partner and dependents.</li>
 <li>Paid sick leave.</li>
 <li>Group life cover.</li>
 <li>Annual leave of 23 days plus bank holidays increasing with service.</li>
 <li>Active Sports and Social Committee with a schedule of events taking place during the year.</li>
 <li>Hybrid working.</li>
 <li>Flexible start and finish times.</li>
 <li>Opportunities for further education, training and development.</li>
 </ul> 
 
 Company Values
 <ul>
 <li>Collaborative</li>
 <li>Innovative</li>
 <li>Empowering</li>
 <li>Patient-centric</li>
 <li>Acting with Integrity</li>
 </ul> 
 
 We retain your details for a period no longer than required for the application process. This allows us to process your details for the purposes of submitting, evaluating, and progressing your application, and any feedback thereafter. If you believe that any of these purposes are overridden by your interests, or fundamental rights and freedoms, please contact us at privacy@veryanmed.com.
 
 When you initially contact us, we retain your data under Article 6(1)(a) Consent, and you have the right to request that this data is deleted. During the application period, we process your data under the legal basis of Article 6(1)(b) Performance of a Contract.
 
 Veryan's recruitment privacy notice is available at https://veryanmed.com/wp-content/uploads/2024/09/Veryan-applicant-privacy-notice-final.pdf
</div>


 R&D Engineer  Full time - Permanent Galway- Hybrid
  We have an exciting opportunity for a R&D Engineer to join Veryan Medical!
   Summary Veryan Medical is a fast-paced, rapidly growing medical device company offering a highly differentiated solution in SFA interventions. We share a commitment, a passion, and a vision for the contribution Veryan makes to innovation in interventional medicine.
  Our team powers Veryan’s business. Whether sales representatives, design engineers, quality engineers, or clinical study managers, our people bring an unmatched expertise in each of their fields that both inspires and challenges.
  Veryan’s culture of innovation helps each individual develop both professionally and personally, and our culture of respect means that we all work in a collaborative, empowering, and exciting environment. We are committed to excellence through our patient-centric approach, and we pride ourselves in our integrity of doing what is right and doing what we say.
  The R&D Engineer will play a key role in Veryan’s current projects and R&D team. This is a great opportunity which will allow the successful candidate to take the next step in their career while working as part of a supportive, collaborative team in the new state-of-the-art facility in Galway.
 
  Job Requirements Principal Responsibilities
 
  Perform project tasks ensuring adherence to the company’s procedures which have been developed in compliance with ISO13485, the Medical Device Directives and FDA 21 CFR 820
  To provide design, development and technical input to the Company’s development projects.
  Packaging development, including design and testing required for new and existing products under development.
  Test method Development, document, training, and validation.
  Support the development of manufacturing processes using tools such as design for six sigma (DFSS) and design for manufacturing (DFM).
  Summarise in vitro test data and communicate the results to project teams leaders and functional groups. Demonstrate a working knowledge of concepts & applications in mechanical and process engineering.
  Using the principles of systematic problem solving, learn and execute analytical techniques such as DOE, Six sigma and statistics.
  Work with the QA Department in developing test, verification and validation (including design review) procedures.
  Manage and co-ordinate procedures, protocols, reports and purchases relevant to the R&D tasks assigned to you, keeping the R&D Project Manager updated.
 
 
  Other duties as required by the Company.
 
 
  Education & Training
 
  Bachelor’s/Master’s degree in Engineering or local equivalent in a scientific discipline and/or appropriate experience.
  Good communication and interpersonal skills.
  Ability to prioritise project tasks and meet deadlines.
 
 
  Experience & Skills
 
  Minimum of one year experience working as an R&D Engineer in the medical device industry.
  Good knowledge of biomechanics and mechanical analysis & design.
  Strong communication skills both written and verbal.
 
 
  Benefits of Working with Veryan:
 
  Competitive salary and bonus.
  Pension scheme with generous employer contributions.
  Private medical insurance for you, spouse / partner and dependents.
  Paid sick leave.
  Group life cover.
  Annual leave of 23 days plus bank holidays increasing with service.
  Active Sports and Social Committee with a schedule of events taking place during the year.
  Hybrid working.
  Flexible start and finish times.
  Opportunities for further education, training and development.
 
 
  Company Values
 
  Collaborative
  Innovative
  Empowering
  Patient-centric
  Acting with Integrity
 
 
 We retain your details for a period no longer than required for the application process. This allows us to process your details for the purposes of submitting, evaluating, and progressing your application, and any feedback thereafter. If you believe that any of these purposes are overridden by your interests, or fundamental rights and freedoms, please contact us at privacy@veryanmed.com.
 
  When you initially contact us, we retain your data under Article 6(1)(a) Consent, and you have the right to request that this data is deleted. During the application period, we process your data under the legal basis of Article 6(1)(b) Performance of a Contract.
 
  Veryan's recruitment privacy notice is available at https://veryanmed.com/wp-content/uploads/2024/09/Veryan-applicant-privacy-notice-final.pdf


R&D Engineer - Veryan Medical

R&D Engineer

You must have a degree in Engineering or related field, 1+ years in medical device R&D, knowledge of ISO13485/FDA standards, strong communication skills, and experience in design/testing.

You will design and develop products, conduct testing, ensure compliance with regulations, manage project documentation, and collaborate with QA and project teams while applying problem-solving techniques.

You need a degree in Engineering or a related field, R&D experience in medical devices, knowledge of biomechanics, and strong communication skills. Prioritization and deadline management are essential.

You will ensure compliance with ISO13485 and FDA standards, develop packaging and test methods, support manufacturing processes, analyze data, and manage R&D documentation.

You must have a degree in Engineering or a related field, 1+ year in medical device R&D, strong communication skills, and a good grasp of biomechanics and mechanical design.

You will perform project tasks, develop designs, manage packaging, summarize test data, collaborate with QA, and utilize problem-solving techniques while adhering to industry standards.

You must have a degree in Engineering, 1+ years in R&D for medical devices, knowledge of ISO13485, strong communication skills, and experience in design, testing, and manufacturing processes.

You will ensure compliance with regulations, contribute to design and development, manage packaging and testing, support manufacturing processes, analyze data, and coordinate R&D tasks.

Veryan Medical

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