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Senior Research And Development Engineer

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Onsite

Senior Research And Development Engineer

ProVerum

Senior Research And Development Engineer

Skills

R

14 days ago

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Important information


Contract type:

Permanent

Salary:

€62,000 – €80,000 / year

Location:

Galway, Ireland

Work mode:

Onsite

Published on:

7 October 2026

What they need


Senior R&D Product Engineer

Location: Galway, Ireland | Full-Time, On-site | Reports to: Senior R&D Manager

ProVerum is transforming the treatment of Benign Prostatic Hyperplasia (BPH) with minimally invasive technology redefining the standard of care. As we scale, we're looking for a Senior R&D Product Engineer to join our R&D team in Galway.

Why ProVerum?

You'll have real ownership, visible impact, and the opportunity to shape the future of BPH treatment, working alongside a team that cares deeply about the patients at the end of every decision.

Why you’ll Thrive?

You're energised by owning a project from the first prototype through to commercial scale-up, and you're happiest when you're hands-on. Reporting to the Senior R&D Manager, you'll work across every stage of device development: prototyping, final manufacture, clinical investigation, commercialisation and scale-up. You'll thrive in a small, entrepreneurial environment where flexibility and cross-functional teamwork are the norm, and where a good attitude and strong work ethic count for as much as your technical skills.

You’ll likely have:

  • A degree in a relevant Engineering or Science discipline, with a minimum of 5 years' experience in the medical device industry
  • Exposure to manufacturing processes for catheters, rigid/flexible endoscopes and/or polymer-based delivery systems
  • Experience in product/process validation and design verification/validation
  • Good mechanical design skills and engineering fundamentals, with strong knowledge of medical device materials (metallic introducers, nitinol and medical device polymers a strong advantage)
  • Good working knowledge of SolidWorks or a comparable CAD package
  • Knowledge of medical device quality and regulatory systems, including ISO 13485 and FDA 21 CFR 820 (a distinct advantage)
  • Excellent communication and technical writing skills
  • Project planning and execution skills (an advantage)
  • A proactive, 'roll-up-your-sleeves' attitude suited to a fast-moving, cross-functional environment

In this role you will:

  • Support and lead R&D projects from concept through to regulatory approval, including project planning and execution
  • Support Operations in sustaining the manufacturing line through real-time troubleshooting during builds, and CAPA and NCR investigations
  • Partner with Operations and Quality to design and optimise manufacturing processes, procedures and production flow
  • Provide technical support to suppliers of components and sub-assemblies to ensure supply reliability, product quality and process consistency
  • Ensure all products, processes and changes comply with QMS and regulatory requirements for PMA and 510(k) products
  • Maintain documentation across production records, DHF, QMS procedures and validation protocols and reports
  • Compile documentation to support sustaining and development activities in line with EU MDR and ISO 13485, including document control and writing protocols and test reports

Why Join the ProVerum Team?

Visible impact from day one: Your work directly supports the devices that reach patients

Build something lasting: Join at a formative stage and help shape the technical foundations of a company

Collaborative culture: Work alongside passionate engineers, technicians, and operators who care deeply about product quality and patient outcomes

Location: Galway's vibrant medtech ecosystem in Ballybrit

Competitive package: Market salary, bonus potential, company pension scheme, private health insurance and more

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