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