Senior Metrology & Validation Engineer for Medical Devices

Gi Group

Leinster

On-site

EUR 65,000 - 90,000

Full time

3 days ago
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Job summary

Gi Group is seeking a Validation & Metrology Engineer to join our quality team in a high-precision medical device environment in Westmeath. The role focuses on owning measurement systems, inspection technologies, and dimensional validation processes.

You will develop metrology solutions, design fixtures, program Micro-Vu systems, perform MSA, and support NPI, validation, and continuous improvement activities within an ISO 13485/FDA-regulated setting.

Qualifications

  • Bachelor's degree in Mechanical/Manufacturing/Quality Engineering or related field.
  • Minimum 5 years' experience in precision metrology or quality engineering.
  • Strong experience programming Micro-Vu systems using MicroView software.
  • Extensive knowledge of optical and tactile CMM inspection techniques.
  • Experience designing metrology and inspection fixtures.

Responsibilities

  • Design, develop and validate custom metrology and inspection fixtures for precision components.
  • Develop, optimise and maintain MicroView programs for Micro-Vu optical CMM systems.
  • Create efficient automated inspection routines for complex machined components.
  • Lead MSA, including Gage R&R, bias, linearity and stability studies.
  • Perform statistical analysis using Minitab to evaluate process capability and measurement performance.
  • Interpret drawings and GD&T per ASME Y14.5.
  • Support FAI, process validation and NPI activities.

Skills

Micro-Vu programming
GD&T
MSA / Gage R&R
CMM inspection fixtures
SolidWorks CAD

Education

Bachelor's Degree in Mechanical Engineering

Tools

SolidWorks
PC-DMIS
Calypso
Mitutoyo MCOS
MicroView software

Job description

Gi Group is seeking a Validation & Metrology Engineer to join our quality team in a high-precision medical device environment in Westmeath. The role focuses on owning measurement systems, inspection technologies, and dimensional validation processes.

You will develop metrology solutions, design fixtures, program Micro-Vu systems, perform MSA, and support NPI, validation, and continuous improvement activities within an ISO 13485/FDA-regulated setting.

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