Process Maintenance Technician

Ballina , Ireland
full-time

AI overview

Play a key role in maintaining production reliability and supporting the development of diagnostic products in a GMP-regulated environment.

We are looking for a Process Maintenance Technician to join our growing team in Ballina, Co Tipperary. This is a hands-on role supporting our manufacturing operations, ensuring equipment runs safely, efficiently, and in line with GMP standards. You’ll play a key part in maintaining production reliability and supporting the development of diagnostic products that help improve patient outcomes around the world.

Key Responsibilities

  • Carry out daily operations, maintenance, and repairs on manufacturing and support equipment within a GMP-regulated environment.
  • Ensure the safe and efficient running of plant equipment, strictly following SOPs, GMP, and quality standards.
  • Identify and solve mechanical and electrical issues on manufacturing and utility equipment in cleanroom environments.
  • Conduct and coordinate preventive maintenance (PM) and work orders (WOs), ensuring accurate documentation and timely progress.
  • Support electrical troubleshooting during equipment faults; identify root causes and implement or coordinate necessary repairs.
  • Liaise with and oversee contractors and vendors as required.
  • Maintain up-to-date knowledge of all relevant SOPs and training requirements to ensure compliance.
  • Interpret P&IDs, wiring diagrams, and equipment layouts to plan and perform maintenance tasks.
  • Promote and maintain a safe working environment in line with company and regulatory safety standards.
  • Occasionally provide technical support to sister companies within the Technopath group.

About You

  • Formal engineering qualification (Diploma or equivalent) with 3–5 years’ experience in a similar role and/or qualified to National Craft Standard.
  • Proven experience working with electrical, pneumatic, and mechanical systems, with strong troubleshooting and problem-solving skills.
  • Experience working in GMP/GDP environments (ISO 9001, ISO 13485, IMB/FDA regulated desirable).
  • Excellent interpersonal and communication skills, both verbal and written.
  • Proficient in Microsoft Office (Outlook, Word, Excel, PowerPoint).
  • Self-motivated with the ability to work independently and take ownership of results.
  • Flexible to support production outside of core hours when required.
  • Experience in Lean manufacturing and/or project management is advantageous.
  • Ability to work effectively within multi-disciplinary teams.
  • Willingness to travel occasionally to provide support at customer or group sites.

Why Join Us?

At LGC Clinical Diagnostics, you’ll be part of a collaborative team that values innovation, precision, and quality. We offer a supportive environment where you can develop your technical expertise, contribute to meaningful work, and grow your career within a global organisation.

Benefits

  • 25 days’ holiday
  • Life assurance and health allowance
  • Discounts with local and national retailers
  • Free 24/7 Employee Assistance Programme
  • Recognition schemes and monetary awards
  • Great long-term career opportunities

Our Commitment

LGC fosters a culture of inclusion, collaboration, and respect. We believe diverse perspectives lead to better outcomes and encourage applications from all backgrounds. We are an equal opportunity employer and provide reasonable accommodations throughout the recruitment process – please let us know if you require any adjustments.

Join us in advancing science and improving lives through diagnostic innovation.

#lgcij

Perks & Benefits Extracted with AI

  • Health Insurance: Life assurance and health allowance
  • Career development opportunities: Great long-term career opportunities
  • Paid Time Off: 25 days’ holiday

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