Overview

Quality Engineer Jobs in Galway Metropolitan Area at ACCPRO

Title: Quality Engineer

Company: ACCPRO

Location: Galway Metropolitan Area

Quality Engineer | Medical Device | Galway | 12-Month Contract

ACCPRO Life Sciences is recruiting a Quality Engineer for a leading medical device manufacturer’s Galway site, on a 12-month contract.

This role sits within a well-resourced quality engineering team, working across packaging and end-of-line operations. You’ll be the go-to person for taking issues from identification through to closure. This includes running CAPAs, supporting process monitoring, and acting as the cross-functional focal point on active investigations, backed by senior quality engineers and a technician team.

Role Responsibilities

  • Formulates procedures, specifications, and standards for products and processes.
  • Provides leadership for quality engineering projects from concept through design, implementation, testing, documentation, support, and maintenance.
  • Develops and implements corrective/preventative action plans.
  • Collects and analyses data for gauge and product evaluation.
  • Develops and maintains an effective and robust quality system which complies with all relevant regulatory requirements.
  • Ensures all validation activity is effective and documented in a compliant manner.
  • Completes in-depth investigations into customer complaints and implements corrective and preventative actions, as appropriate.
  • Identifies critical personnel, gauges, procedures, and materials needed for the completion of new products.
  • Ensures that suppliers have necessary information and facilities to deliver quality products. Evaluates new suppliers as required and coordinates supplier corrective actions where necessary. Ensures that the Receiving Inspection process is implemented in a compliant and effective manner.

What you’ll need:

  • Clean room experience — ideally in packaging or end-of-line manufacturing
  • A track record of owning issues/CAPAs through to closure
  • Medical device experience is a strong plus, but we’re equally interested in strong QMS backgrounds from other regulated industries

Requirements

  • Third-level Engineering or Science degree. Certification as a Quality Engineer (e.g. CQE) is preferred.
  • 5+ years’ experience in a Quality Engineering role.
  • Travel requirements up to 20%.
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