Location: Galway or Dublin, Ireland | Full-Time, On-site | Reports to: Quality Director
ProVerum is changing how Benign Prostatic Hyperplasia (BPH) is treated, pioneering minimally invasive technology that sets a new standard of care. As we scale, we're looking for a Quality Systems Engineer to join our Quality team in Galway or Dublin.
YOUR ROLE AT PROVERUMReporting to the Quality Director, you’ll play a central role in maintaining and evolving our Quality Management System, supporting regulatory compliance, supplier quality, and audit readiness as we grow, commercialise and improve patients’ lives.
WHAT YOU WILL NEEDQualifications & Experience
Bachelor’s degree in Engineering or a relevant Science field
Minimum 3 years’ experience in the medical device industry (or equivalent postgraduate study, Master’s / PhD)
Lead Auditor certification (preferred)
Strong knowledge of ISO 13485 and FDA 21 CFR 820 (essential)
Skills & Approach
Hands-on, motivated, and proactive, you take initiative and follow through
Strong written and verbal communication skills; confident producing procedures, plans, and reports
Comfortable working in a fast-moving, small team environment where flexibility matters
Maintaining and continuously improving quality policies, procedures, change control, and training
Supporting complaint handling, CAPAs, and NCRs
Leading and supporting internal, supplier, and regulatory agency audits (FDA, Notified Body)
Contributing to eQMS and ERP platform implementation projects
Developing quality plans and procedures to support commercialisation
Visible impact from day one: your work directly supports the devices that reach patients
Build something lasting: join at a formative stage and develop deep SME-level expertise
Collaborative culture: work with people who care deeply about quality and patient outcomes
Competitive package: market salary, bonus potential, company pension, private health insurance and more
You’ll support the full breadth of our QMS activities, including:
Maintaining and continuously improving quality policies, procedures, change control, and training
Supporting complaint handling, CAPAs, and NCRs
Leading and supporting internal, supplier, and regulatory agency audits (FDA, Notified Body)
Contributing to eQMS and ERP platform implementation projects
Developing quality plans and procedures to support commercialisation
Visible impact from day one: your work directly supports the devices that reach patients
Build something lasting: join at a formative stage and develop deep SME-level expertise
Collaborative culture: work with people who care deeply about quality and patient outcomes
Competitive package: market salary, bonus potential, company pension, private health insurance and more
Skills Required
- Bachelor’s degree in Engineering or a relevant Science field
- Minimum 3 years’ experience in the medical device industry, or equivalent postgraduate study such as a Master’s or PhD
- Lead Auditor certification
- Strong knowledge of ISO 13485
- Strong knowledge of FDA 21 CFR 820
- Strong written and verbal communication skills
- Ability to produce procedures, plans, and reports
- Experience maintaining and improving quality policies, procedures, change control, and training
- Experience supporting complaint handling, CAPAs, and NCRs
- Experience leading or supporting internal, supplier, and regulatory agency audits
- Experience contributing to eQMS and ERP platform implementation projects
What We Do
Focused on the development of minimally invasive technologies to treat BPH.
