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Medical Devices jobs in County Galway

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    • Perform incoming, in-process, and final inspections of medical device components and finished products.
    • Minimum 1–3 years’ experience in a Quality or Inspection…
    • Significant experience within a GMP pharmaceutical, sterile manufacturing, biologics, or medical device microbiology laboratory.
    • Have working knowledge of MODA.
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    • Strong experience in sterile pharmaceutical and/or medical device manufacturing.
    • The Associate Quality Director / QP has responsibility for administration of…
    • The Quality Assurance Documentation Controller will be responsible for the day to day management of the site GMP documentation system, acting as administrator…
    • On-device analytics: a CoreML (iOS) / TFLite (Android) inference runtime for health metrics such as sleep quality, HRV, and activity; bridging model outputs…
    • Manufacturing, medical device or SME experience.
    • Work in a modern, high-precision medical device manufacturing environment.
    • Job Types: Permanent, Full-time.
    • Lead and support a team of Manufacturing Engineers and Technicians, helping to build capability and ensure strong integration with the wider production team.
    • Good working knowledge of ISO 13485, FDA requirements and medical device Quality Systems.
    • Take ownership of quality activities across manufacturing, ensuring…
    • In this role you will be operating within the production floor, performing the following activities: CNC Machining, NDT Inspection, Robotic Finishing, and…
    • Manpower Group Ireland Ltd are looking to recruit a number of Product Builders for either Fixed Day or Fixed Night Shifts for our client Zimmer Biomet in…
    • Manpower Group Ireland Ltd are looking to recruit a number of Product Builders for Weekend Night Shifts for our client Zimmer Biomet in Oranmore Co. Galway.
    • 5+ years' experience in an EHS leadership role within construction, manufacturing, engineering, pharmaceutical, medical device or industrial environments.
    • Applies scientific and engineering knowledge to the development and improvement of medical device products, associated processes, and manufacturing equipment as…
    • Assemble, inspect, test and operate equipment to manufacture products.
    • Inspect and test products and check statistical process control.
    • This role is based in the company’s European facility in Athenry on our evening shift.
    • Evening shift hours are Monday - Thursday 4pm - 12:30am and *1:30pm…

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Job Post Details

Quality Technician - job post

Cregg Recruitment Ltd
4.4 out of 5 stars
Galway, County Galway

Location

Galway, County Galway

Full job description

Quality Technician

CREGG are hiring for a Quality Technician for a leading Medical Device Company in Galway.

For more information contact mark: 086 190 1346 or markhalligan@cregg.ie

Job Summary

The Quality Control Inspector is responsible for ensuring that products meet established quality standards and regulatory requirements throughout the manufacturing process. This role supports compliance with ISO 13485, FDA QSR (21 CFR Part 820), and EU Medical Device Regulations (MDR), while contributing to continuous improvement and patient safety.

Key Responsibilities

  • Perform incoming, in-process, and final inspections of medical device components and finished products

  • Conduct visual, dimensional, and functional inspections using appropriate measuring equipment (e.g., calipers, micrometers, gauges, optical comparators)

  • Review and interpret engineering drawings, specifications, and inspection plans

  • Accurately document inspection results in accordance with GMP and company procedures

  • Identify, document, and report non-conformances; support investigations and corrective actions (CAPA)

  • Ensure compliance with ISO 13485, FDA, EU MDR, and internal quality system requirements

  • Support lot release activities and ensure traceability of inspected materials

  • Participate in audits (internal, customer, and regulatory) as required

  • Maintain inspection equipment and ensure calibration status is up to date

  • Contribute to continuous improvement initiatives within the Quality function

  • Adhere to health, safety, and environmental requirements at all times

Requirements & Qualifications

Essential:

  • Leaving Certificate or equivalent qualification (FETAC/QQI Level 5 or higher preferred)

  • Minimum 1–3 years’ experience in a Quality or Inspection role within a regulated manufacturing environment (medical device, pharmaceutical, or life sciences preferred)

  • Strong understanding of GMP and quality systems

  • Ability to read and interpret technical drawings and specifications

  • High attention to detail and strong documentation skills

  • Good written and verbal communication skills

  • Ability to work independently and as part of a team

    INDTRAC

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