Medical Devices JobsQuality Engineer

  • 50368
  • Permanent
  • Offaly

Collins McNicholas

As part of this role, you will be responsible for and has the authority for product/process quality improvement programmes, analysis of quality costs, customer complaints, analysis of quality waste, reliability evaluations and process capabilities studies.

Quality Engineer Responsibilities:

  • Lead quality improvement programmes using recognised problem-solving and project management techniques
  • Evaluate quality trends and reasons for product or process failures relating to customer complaints and lead corrective action plans.
  • Evaluate quality costs and determine critical causes.
  • Prepare and approve quality assurance specifications and assist in the formulation of written policy/procedures
  • Align and integrate company test procedures with International Standards requirements.
  • Assist in determining inspection frequencies and sampling plans using significance testing, capability studies and through collation and analysis of data
  • Participate in the validation of all new tooling equipment, methods and products.
  • Ensure all areas comply with specified regulatory requirements
  • Any other reasonable duties as required

Quality Engineer requirements:
▪ Third level qualification in science/ engineering.
▪ Three years’ experience in Quality Engineering in a manufacturing environment
▪ Demonstrable Lean/ Six Sigma certification is an advantage
▪ Strong analytical skills, including statistical analysis is an advantage

For a confidential discussion and more information on the role, please contact Tina Egan

09064 78104

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