Manufacturing Engineering Lead – Automated High-Volume Ops

Boston Scientific

Cork

On-site

EUR 65,000 - 90,000

Full time

37 hours ago
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Job summary

Boston Scientific Cork seeks an Associate Manufacturing Engineer to lead a high-volume, highly automated value stream. You will develop engineering capability, drive equipment reliability, and guide validation and process improvements while prioritising patient safety and product quality.

The role requires strong problem-solving, Lean Six Sigma experience, and a track record of cross-functional leadership within a regulated manufacturing environment.

Qualifications

  • Honors degree in engineering or STEM.
  • Minimum 5 years in manufacturing engineering or related field.
  • Experience leading engineers and technical teams.
  • Strong knowledge of automated manufacturing equipment and controls.
  • Experience in validated quality systems and process improvement.

Responsibilities

  • Provide engineering leadership for highly automated lines with near 24/7 operation.
  • Coach and develop Manufacturing Engineers and technical resources.
  • Own equipment health, reliability and capacity planning for the value stream.
  • Lead root-cause analysis and corrective actions for complex issues.
  • Drive OEE, throughput, cycle time, yield and process capability improvements.
  • Oversee qualification, validation and change control activities.
  • Collaborate with Operations, Quality, Process Development and Maintenance.
  • Lead capital equipment projects from requirements to production handover.
  • Ensure safety, quality and compliance in all manufacturing activities.

Skills

Leadership
Problem-solving
Quality systems
Lean Six Sigma
Automation/controls
Cross-functional collaboration
Communication

Education

Honors Bachelors Degree (Level 8) in engineering or related STEM

Job description

Boston Scientific Cork seeks an Associate Manufacturing Engineer to lead a high-volume, highly automated value stream. You will develop engineering capability, drive equipment reliability, and guide validation and process improvements while prioritising patient safety and product quality.

The role requires strong problem-solving, Lean Six Sigma experience, and a track record of cross-functional leadership within a regulated manufacturing environment.

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