Senior NPD Engineer — Lead Medical Device Development

Hero Recruitment Group

Galway

On-site

EUR 80,000 - 90,000

Full time

9 days ago
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Job summary

Hero Recruitment Group is seeking a Senior NPD Engineer in Galway to provide technical leadership across development programs, owning engineering execution from feasibility through manufacturing transfer.

The ideal candidate has a mechanical/biomedical/polymer engineering background with 7+ years in medical device development, strong customer-facing project leadership, and familiarity with Design Control, ISO 13485, and FDA requirements.

Qualifications

  • Bachelor's degree in Mechanical, Biomedical, Polymer Engineering, or related discipline.
  • Minimum 7 years' medical device product development experience.
  • Experience leading development projects within Design Control and regulated environments.
  • Proven customer-facing experience with technical discussion and project leadership.
  • Knowledge of ISO 13485 and FDA requirements.
  • Catheter-based or delivery system technology experience is an advantage.

Responsibilities

  • Lead technical execution of product development programs from feasibility through manufacturing transfer.
  • Act as primary technical interface with customers, leading design reviews and problem-solving activities.
  • Own technical strategy and engineering execution for assigned projects.
  • Partner with Program Managers on planning, budgeting, and risk management.
  • Drive development through verification, validation, design transfer, and commercialisation.
  • Provide leadership, coaching, and technical guidance to engineers and technicians.

Job description

Hero Recruitment Group is seeking a Senior NPD Engineer in Galway to provide technical leadership across development programs, owning engineering execution from feasibility through manufacturing transfer.

The ideal candidate has a mechanical/biomedical/polymer engineering background with 7+ years in medical device development, strong customer-facing project leadership, and familiarity with Design Control, ISO 13485, and FDA requirements.

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