Automation Technician - Manufacturing 
We are seeking a motivated Project/Automation Engineer to support the development of new technology and optimize existing systems to enhance production, quality, profitability, and safety.

This role involves the planning, scheduling, and execution of projects, ensuring delivery within committed timelines. You will also contribute to facility expansions and modifications, working closely with engineering management and production support teams.

Kay Responsibilities

• Support the development of new and existing technology and production lines to improve efficiency, quality, and safety.
• Plan, execute, and document project assignments in line with governance policies, timelines, and project goals.
• Ensure all technical and customer requirements are achieved.
• Develop and maintain validation and project management documentation.
• Participate in regular project reviews with teams and management.
• Perform design work, layouts, sketches, and concepts for projects and plant layouts.
• Review and develop engineering change requests for modifications to processes, equipment, and facilities.
• Troubleshoot and repair automation equipment.
• Evaluate and maintain machine safety systems to protect operators.
• Monitor production data to ensure automation lines achieve targeted OEE and output.
• Maintain product quality through effective automation maintenance and operation.
• Provide timely updates to shift leaders and program managers regarding downtime or maintenance issues.
• Interface daily with the Engineering Manager and shift support staff.
• Ensure compliance with all safety, regulatory, and quality standards.
• Support and maintain automation equipment, including: Assembly machines/fixtures, Label applicators, Robots and end of arms, Separators, Test equipment & Other assigned equipment

• Associate’s Degree in a relevant Engineering discipline (required).
• Bachelor’s Degree in a relevant Engineering discipline (preferred).
• Minimum 3 years’ experience in the medical device or other regulated industry (required).
• Minimum 3 years’ experience supporting technical project management (preferred).

• Background in medical devices/pharmaceuticals is a plus.
• Strong knowledge of quality systems requirements, FDA QSR, cGMP, and relevant ISO standards.
• Travel & Physical Requirements
• Travel: Up to 5% (approx. 13 business days per year).
• Ability to exert up to 20lbs/9kg of force frequently.
• Must be able to work a standard 40-hour week, with overtime/irregular hours as required.
• May require standing or sitting for extended periods.
• Must tolerate manufacturing environment conditions (plastic injection molding, fumes, particulates).

For further information on this role in please contact on Gavin Moran on 087 4108620 or connect@hero.ie

Check out all our open jobs on our HERO Recruitment website – https://www.hero.ie/

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Data can only be transferred outside of the EEA on the basis of standards contractual clauses, to a country for whom an adequacy decision has been given by the European Commission or where the express permission of the data subject has been given. You have supplied us with your personal data in the process of applying for a position. Our client company may have personnel outside of the EEA who will review