NPI / Product Transfer Engineer

Location: Galway

Schedule: Full-time, weekdays

A leading Galway-based medical device manufacturer is seeking an experienced NPI / Product Transfer Manufacturing Engineer to join its expanding Engineering team. This is a newly created role within a core engineering group, focused on supporting the successful introduction and transfer of innovative medical technologies into full-scale commercial manufacturing. The successful candidate will play a key role in establishing robust, efficient, and compliant production processes, working cross-functionally to ensure a smooth transition from development through to commercialisation. This hands‑on engineering role requires strong technical capability, structured problem‑solving skills, and experience in validation within a regulated manufacturing environment.

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• Support and lead assigned engineering activities within NPI and product transfer projects.
  
• Establish robust and repeatable manufacturing process controls.
  
• Drive process optimisation and performance improvements using structured CI methodologies.
  
• Apply scientific and data‑driven problem‑solving approaches to improve yield and efficiency.
  
• Ensure compliance with GMP, regulatory, quality, and EHS standards.
  
• Collaborate with automation and technical teams to develop stable and capable processes.
  
• Support new technology introductions and effective engineering change management.
  
• Lead and execute equipment and process validations (IQ, OQ, PQ).
  
• Investigate and resolve non‑conformances in line with quality systems.
  
• Contribute to risk assessments (process, equipment, and product).
  
• Develop technical expertise across core manufacturing technologies.
  

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• Level 8 Honours Degree in Engineering (or equivalent technical discipline).
  
• 3–5+ years’ experience in a Manufacturing Engineering role within medical device or regulated healthcare manufacturing.
  
• Proven experience supporting NPI, product transfer, or scale‑up activities.
  
• Strong validation experience (IQ/OQ/PQ).
  
• Experience implementing continuous improvement initiatives.
  
• Knowledge of regulatory and quality requirements in a regulated environment (e.g., ISO standards).
  
• Strong documentation and technical report writing skills. xcfaprz
  
• Proficiency in CAD is advantageous.
  

For further information on this role, please contact Gavin Moran on or via email at

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