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    • Previous experience within medical devices, pharmaceuticals, biotechnology, or another regulated manufacturing environment.
    • Shift: Day Shift (Monday to Friday).
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Job Post Details

Manufacturing / Design & Development Engineer I
CPL
·
3.4
County Galway
€41,000–€51,000 a year
Fixed term

Job details

€41,000–€51,000 a year
Fixed term
Day shift, Monday to Friday
County Galway

Full job description

Manufacturing / Design & Development Engineer I

Location: Galway (Fully Onsite)

Contract Duration: 12 Months

Salary: €41,000 - €51,000

Hours: 40 Hours per Week

Shift: Day Shift (Monday to Friday)

About the Role

Our client, a leading multinational medical device organisation, is seeking a Manufacturing / Design & Development Engineer to join their Galway-based team on a 12-month contract.

This opportunity is ideal for a graduate engineer or an engineer in the early stages of their career who is looking to gain valuable experience in manufacturing engineering, process development, and continuous improvement within a highly regulated environment.

The successful candidate will support manufacturing operations, drive process improvements, and collaborate with cross-functional teams to ensure efficient and compliant production processes.

Key Responsibilities

  • Provide technical and sustaining engineering support within a manufacturing environment.
  • Support continuous improvement initiatives focused on quality, efficiency, and yield enhancement.
  • Recommend and implement equipment, tooling, fixture, and process improvements.
  • Assist in the development, optimisation, and transfer of manufacturing processes into production.
  • Collaborate with R&D, quality, and manufacturing teams to support new product introduction activities.
  • Conduct process investigations, root cause analysis, and corrective actions.
  • Support equipment installation, qualification, and validation activities.
  • Develop and apply statistical process control methodologies where appropriate.
  • Prepare and maintain engineering documentation and technical reports.
  • Ensure compliance with quality systems, regulatory requirements, and company procedures.

Qualifications & Experience

Essential

  • Bachelor's Degree in Engineering or a related technical discipline.
  • Strong understanding of engineering and manufacturing principles.
  • Excellent analytical and problem-solving skills.
  • Strong communication and interpersonal skills.
  • Ability to work effectively in a team-oriented environment.

Desirable

  • Previous experience within medical devices, pharmaceuticals, biotechnology, or another regulated manufacturing environment.
  • Exposure to process development, manufacturing engineering, or product development activities.
  • Knowledge of:
    • Statistical Process Control (SPC)
    • Lean Manufacturing methodologies
    • Validation and qualification processes
    • Root Cause Analysis tools and techniques

Key Competencies

  • Technical Problem Solving
  • Continuous Improvement
  • Process Optimisation
  • Data Analysis
  • Attention to Detail
  • Team Collaboration
  • Quality & Compliance Focus
  • Effective Communication

What's on Offer

  • 12-month contract opportunity.
  • Competitive salary of €41,000 - €51,000.
  • Opportunity to gain experience with a world-class medical technology organisation.
  • Exposure to advanced manufacturing and engineering projects.
  • Collaborative and innovative working environment.
  • Fully onsite role based in Galway.

For discreet enquiries please email your CV to morgan.danaher@cpl.ie or call me on 0871647527

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