Manufacturing Engineer II – Medical Device Improvement

TE Connectivity Ltd.

Galway

On-site

EUR 55,000 - 75,000

Full time

2 days ago
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Benefits offered by this job

Competitive Salary Package
Performance-Based Bonus Plans
Health and Wellness Incentives
Employee Stock Purchase Program
Community Outreach Programs / Charity

Job summary

TE Connectivity plc in Galway, Ireland is seeking a Manufacturing Engineer II to sustain and improve existing medical device production. You will troubleshoot issues, drive process improvements, and support ongoing production while ensuring regulatory and quality standards are met.

Qualifications include an Engineering degree (Level 8) and a minimum of 3 years’ experience. Strong problem-solving, communication, and cross-functional collaboration skills are essential.

Qualifications

  • Engineering degree (Level 8) or equivalent.
  • Preferably 3 years’ experience in a similar role.
  • Strong problem-solving and troubleshooting skills with a proven track record.
  • Ability to prioritize tasks and manage multiple projects.
  • Excellent communication and collaboration skills for cross-functional work.
  • Knowledge of lean manufacturing and statistics is advantageous.

Responsibilities

  • Provide day-to-day technical support to resolve production challenges and minimize downtime.
  • Analyse root causes of issues and implement corrective actions to address defects.
  • Identify opportunities to improve yields and reduce waste using Lean/Six Sigma.
  • Lead or support engineering changes (ECOs) and validate documentation.
  • Maintain equipment through preventative maintenance and upgrades.
  • Collaborate with Quality, Operations and Supply Chain to address deviations.

Skills

Problem-solving
Troubleshooting
Communication
Collaboration
Critical thinking
Attention to detail
Data-driven

Education

Engineering degree (Level 8)

Tools

Minitab
SolidWorks
AutoCAD

Job description

TE Connectivity plc in Galway, Ireland is seeking a Manufacturing Engineer II to sustain and improve existing medical device production. You will troubleshoot issues, drive process improvements, and support ongoing production while ensuring regulatory and quality standards are met.

Qualifications include an Engineering degree (Level 8) and a minimum of 3 years’ experience. Strong problem-solving, communication, and cross-functional collaboration skills are essential.

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