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Manufacturing Engineer 2

Limerick, Limerick
Role Type
Regina Carroll
+353 86 010 0903
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Manufacturing Engineer 2

Similar Jobs
Manufacturing Engineer 2

Our client is a leading Medical Device Manufacturer, based centrally in Limerick.  This role is an 18 month fixed term contact offering competitive salary and all company benefits. 


Process Improvement

  • Lead projects to implement process changes for improved device quality, performance, and cost reduction.
  • Identify and drive yield and efficiency improvement opportunities.
  • Provide engineering input for resolving Non-Conformances and regulatory submissions.
  • Collaborate with R&D and Process Development for smooth device transfers.
  • Develop and implement engineering layout plans for line extensions or redesigns.
  • Participate in CAPA, Design, Manufacturing, EHS, or NPI projects.
  • Lead or support Continuous Improvement activities to enhance key business metrics.
  • Develop project deliverables such as BOMs and production documentation.

Production Maintenance

  • Develop and implement maintenance strategies for production equipment.
  • Ensure Preventative Maintenance and Calibration activities optimize equipment performance.
  • Plan and schedule maintenance tasks with Operations.
  • Conduct tooling criticality assessments and manage equipment in the INFOR EAM system.
  • Resolve equipment issues through Green Belt or Problem-Solving events.
  • Source and install new equipment as per quality systems.
  • Develop jigs, fixtures, and tooling to improve efficiencies.
  • Define maintenance and calibration requirements for new and existing equipment.
  • Conduct time studies and generate standard work instructions.
  • Plan and execute improvement projects to meet timelines, quality, and cost targets.

New Product Introduction

  • Lead or support process development activities for New Product Introduction (NPI).
  • Ensure new products follow DFM principles and integrate with current systems.
  • Define Bills of Materials and product capacity requirements.
  • Drive project tasks to meet milestones and business metrics.
  • Provide technical expertise for regulatory submissions and renewals.

Qualifications / Requirements:

  • Bachelor's degree in engineering or related field preferred, with 3+ years relevant experience.
  • Strong interpersonal, organizational, and project planning skills.
  • Proven problem-solving abilities and high motivation for excellence.
  • Experience in medical device quality and regulatory systems preferred.
  • Proficient in Microsoft Office and willing to travel as needed.

For further information on this role please contact Regina Carroll  call 086 0100 903 or email

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Please Note: Under its obligation under the Data Protection legislation, HERO Recruitment will not forward your details to any company without your prior approval.

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 you data. We will apply the appropriate criteria in respect of the data transfer depending on the location of those personnel.

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