CPL

Automation Engineer - Tipperary

View CPL profile
Location
Clonmel, Co. Tipperary
Location type
At the office
Employment type
Full time
Job type
Permanent
Salary
Negotiable
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Automation Engineer – Medical Device Sector

Location: On-site, Ireland

Work Authorisation: Must hold Stamp 4 or have full, unrestricted working rights in Ireland.

Our client is a global leader in the medical device industry, known for innovation, quality, and delivering life-changing technology. They are seeking an experienced Automation Engineer to join their team, supporting both manufacturing and R&D projects on-site.

This is a hands-on role with involvement in design, development, implementation, and optimisation of automation systems to improve efficiency, productivity, and compliance within a regulated environment.

Key Responsibilities

Automation System Design & Development

  • Design and develop automation systems and processes for manufacturing and R&D.
  • Identify opportunities to streamline operations, reduce waste, and increase throughput.
  • Integrate automation solutions with existing equipment and systems.

Project Collaboration & Planning

  • Work closely with project managers, engineers, and stakeholders to define requirements.
  • Create detailed project plans, including scope, timelines, budgets, and resources.
  • Conduct feasibility studies and risk assessments for proposed solutions.

Installation, Testing & Commissioning

  • Oversee the installation of automation equipment.
  • Manage testing and commissioning to ensure operational readiness.
  • Coordinate with suppliers, contractors, and internal teams for seamless delivery.

Troubleshooting & Continuous Improvement

  • Diagnose and resolve technical issues with automation hardware and software.
  • Implement preventative maintenance and reliability improvements.
  • Analyse system performance and recommend enhancements.

Compliance & Documentation

  • Ensure all automation systems comply with medical device regulations, safety standards, and company policies.
  • Develop and maintain technical documentation, including:
    • User manuals
    • Maintenance procedures
    • Project reports
  • Support internal and external audits as required.

Training & Support

  • Train end-users and maintenance teams on system operation.
  • Provide ongoing technical support to ensure smooth production and R&D workflows.

Qualifications & Experience

  • Education: NFQ Level 7 qualification (180 credits) in Automation, Mechatronics, Electrical, or related discipline.
  • Industry Experience: Proven track record in automation engineering, ideally in the medical device sector or other regulated manufacturing environments (e.g., pharma, biotech).
  • Technical Skills:
    • PLC programming (e.g., Siemens, Allen-Bradley, or similar)
    • HMI development
    • SCADA systems integration
    • CAD software proficiency (AutoCAD, SolidWorks, or equivalent)
    • Familiarity with industrial networking and control systems
  • Soft Skills:
    • Strong problem-solving and analytical skills
    • Excellent communication and stakeholder engagement
    • Ability to work both independently and as part of a cross-functional team
  • Desirable:
    • Project Management Certification (PMP or equivalent)
    • Experience with validation and documentation in regulated industries

What’s on Offer

  • Opportunity to work with a global leader in a high-growth sector.
  • Exposure to cutting-edge automation and medical device technology.
  • Collaborative and innovative work culture.
  • Career progression and professional development opportunities.

#LI-DB4

Important Dates
Posted on
18 August, 2025
Reference number
JO-2508-555429

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