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Medical Devices jobs in Waterford, County Waterford

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    • Support IQ, OQ, and PQ activities in compliance with medical device regulatory requirements.
    • We are seeking an experienced Automation Engineer to support the…
    • 5+ years’ experience working within a GMP-regulated pharmaceutical, biotechnology or medical device manufacturing environment.
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    • Previous internship, placement, research, or work experience within a regulated industry such as pharmaceuticals, biotechnology, medical devices, or healthcare.
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    • Experience in pharmaceutical, medical device, or other regulated manufacturing environment.
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    • Previous pharmaceutical, biotech, medical device or sterile manufacturing experience is highly desirable.
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Job Post Details

Automation Engineer
Waterford, County Waterford
€58,000–€65,000 a year
Full-time

Job details

€58,000–€65,000 a year
Full-time
Waterford, County Waterford

Full job description

We are hiring a Automation Engineer on behalf of our client in Waterford.

Role Summary

We are seeking an experienced Automation Engineer to support the design, development, implementation, and validation of automated manufacturing equipment within a regulated medical device manufacturing environment. The successful candidate will have a strong background in industrial automation, robotics, and machine design, with proven experience delivering automated production cells from concept through release.

Key Responsibilities

  • Design, develop, and implement automated manufacturing solutions to improve safety, quality, capacity, and efficiency.
  • Program, troubleshoot, and optimize PLC-controlled equipment.
  • Design and integrate robotic automation systems, including Universal Robots (UR).
  • Configure, deploy, and support Mobile Industrial Robots (MiR) for material handling and logistics applications.
  • Lead automation projects from concept, design, build, testing, validation, and production handover.
  • Develop machine control architectures, electrical schematics, and functional specifications as requyired.
  • Support IQ, OQ, and PQ activities in compliance with medical device regulatory requirements.
  • Troubleshoot production equipment and implement corrective actions to minimize downtime.
  • Collaborate with Manufacturing, Quality, Validation, and Production teams on continuous improvement initiatives.
  • Ensure automation systems comply with machine safety and risk management requirements.

Pay: €58,000.00-€65,000.00 per year

Work Location: In person

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