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Biomedical jobs in Galway, County Galway

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    • Be part of a growing organization committed to quality, innovation, and compliance with international standards such as ISO 13485, FDA 21 CFR Part 820, and EU…
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    • The successful candidate will be responsible for providing daily support of and equipment, processes, materials, in order to achieve production goals along with…
    • The successful candidate will be responsible for providing daily support of and equipment, processes, materials, in order to achieve production goals along with…
    • BE + ME Mechanical Engineering.
    • BE + ME Electronic & Computer Engineering.
    • Provide daily technical support to the department.
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    • BE + ME Mechanical Engineering.
    • Provide daily technical support to the department.
    • Carry out a project and report progress as agreed by Supervisor/Manager.
    • I am currently working on behalf of a client within the medical technology sector to recruit a Technical Business Development Manager to join their team.
    • We are seeking a motivated R&D Engineer to support the development and improvement of disposable medical devices, including EEG cup electrodes, needle…
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    • The Manufacturing Engineer supports the design, development, validation, and continuous improvement of manufacturing processes for medical devices.
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    • The successful candidate will partner with R&D, Manufacturing, Quality, and Regulatory Affairs teams to ensure medical devices are designed, developed, verified…
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    • The successful candidate will partner with R&D, Manufacturing, Quality, and Regulatory Affairs teams to ensure medical devices are designed, developed, verified…
    • Successful candidates come from a strong project leadership/validation/equipment or medical device background.
    • Provide leadership on Lean initiatives.
    • Join our Engineering team to provide technical leadership in the development, validation and continuous improvement of additive manufacturing technologies that…
    • The Senior Manufacturing Engineer will play a critical role in supporting the manufacturing operations of our medical device products.
    • The Quality Engineer is responsible for ensuring the quality, compliance, and continuous improvement of medical device products and processes throughout the…
    • J.E. Cairnes School of Business & Economics, University of Galway.
    • Ref. No. University of Galway 002-25.
    • ROSETTA fellows will be provided with the highest…

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Manufacturing Engineer
Sigmar
·
4.3
Galway, County Galway
Full-time

Job details

Here’s how the job details align with your profile.

Job type

Full-time

Full job description

Manufacturing Engineer

About Your New Employer

  • Join a pioneering company in the development of advanced medical devices for global markets.
  • Work at the forefront of medical technology with a highly skilled, cross-functional team and a strong culture of continuous improvement.
  • Be part of a growing organization committed to quality, innovation, and compliance with international standards such as ISO 13485, FDA 21 CFR Part 820, and EU MDR directives.
  • This job is fully onsite.

About Your New Job

As a Manufacturing Engineer, you will:

  • Provide ongoing engineering support to the manufacturing line, ensuring efficient and stable operations.
  • Lead troubleshooting and root cause analysis for complex equipment, processes, or material issues, implementing effective corrective and preventive actions (CAPAs).
  • Manage process and equipment change control, including all validation and associated documentation, per rigorous QMS and regulatory standards.
  • Identify and deploy new tools, jigs, fixtures, or process solutions to improve manufacturing efficiency, product quality, and reliability.
  • Drive and deliver continuous improvement initiatives using Lean Manufacturing, Six Sigma, or other recognized methodologies.
  • Collaborate with multidisciplinary teams in risk management, process development, and equipment or product validation projects (IQ, OQ, PQ).
  • Develop, review, and maintain technical documentation, SOPs, work instructions, and visual standards.
  • Ensure a GMP-compliant, safe, and orderly work environment, and support ongoing staff training on manufacturing processes.

What Skills You Need

  • Bachelor’s degree in Engineering (Mechanical, Manufacturing, Biomedical, or related disciplines).
  • 3–5 years of hands-on experience in the medical device or pharmaceutical industry, with a background in production equipment operation/maintenance and process improvement.
  • Sound knowledge of ISO 13485, MDR, and FDA regulatory requirements; experience working within a QMS.
  • Strong analytical and troubleshooting skills, ownership mentality, and ability to work both autonomously and collaboratively.
  • Proficiency in process improvement tools (Lean, Six Sigma—Green Belt an advantage).
  • Excellent communication, teamwork, and documentation capabilities.
  • Strong organizational skills and ability to juggle multiple priorities in a fast-moving production environment.

What's on Offer

  • Competitive salary, commensurate with experience.
  • Opportunities for ongoing career growth, professional development, and training (including further Lean/Six Sigma certification).
  • Be part of innovative teams driving exciting product development projects and see your impact on products that matter.
  • Comprehensive benefits package.

What's Next

Apply now by clicking the “Apply Now” button or reach out to us directly for more information. If this role isn’t quite right, but you are seeking something similar within medical device engineering, please get in touch—we have multiple opportunities available.

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