- ProVerum
- Galway, Connacht
- Full-Time
- 47 days ago
Senior Product Engineer.
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Senior Product Engineer: our view in 3 lines...
- The Role:This role is for a senior engineer in medical devices focused on product development and manufacturing support for a minimally invasive treatment for BPH.
- The Person:The person will support manufacturing, troubleshoot issues, drive root cause investigations, improve processes, support suppliers, and maintain validation and quality documentation.
- Requirements:The ideal candidate has a bachelor’s degree in engineering or a related technical field, at least 5 years’ experience in the medical device industry, and working knowledge of SolidWorks, ISO 13485, and FDA 21 CFR 820.
About the role
Senior 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 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 the intersection of engineering rigour and real-world product impact, and you're comfortable being the technical go-to person across functions. You thrive in environments where problems are complex, stakes are high, and your work directly influences patient outcomes.
You’ll likely have:
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A minimum bachelor’s degree in a relevant Engineering or a related technical field, with a minimum of 5 years' experience in the medical device industry
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Exposure to manufacturing processes for catheters and/or polymer-based delivery systems and injection moulding
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Demonstrated analytical problem-solving abilities, you're methodical under pressure and comfortable driving investigations through to root cause
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Experience in product/process validation and design verification/validation
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Strong knowledge of medical device materials, nitinol and medical device polymers a strong advantage
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Good working knowledge of SolidWorks or a comparable CAD package
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Knowledge of medical device quality and regulatory systems, including ISO 13485 and FDA 21 CFR 820
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Excellent communication and technical writing skills
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Project planning and execution skills
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A proactive, 'roll-up-your-sleeves' attitude suited to a fast-moving, cross-functional environment
In this role you will:
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Sustain the manufacturing line, real-time troubleshooting, CAPA, NCR, and SCAR ownership through to root cause and corrective action
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Partner with Operations and Quality to design, optimise, and scale manufacturing processes and production flow
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Lead process improvement initiatives, including fixturing/tooling design, verification, and implementation
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Provide technical support to suppliers to ensure supply reliability, product quality, and process consistency
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Support new design evaluation, packaging development, and iteration of existing products and processes
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Ensure all products and changes comply with QMS and regulatory requirements (ISO 13485, PMA, 510k)
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Maintain documentation across DHF, QMS procedures, validation protocols, and production records
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Coach and upskill team members as needed
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

