Senior Industrial Engineer

Johnson & Johnson Innovative Medicine

Santa Clara, California, United States
Base: $109,000.00 - $174,800.00; bonus/equity: not...
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Lean and six sigma methods
Process design and validation
Labor and capacity modeling
** Johnson & Johnson is seeking a Senior Industrial Engineer to lead manufacturing systems and process improvements in Santa Clara, CA. The ideal candidate will have significant experience in regulated manufacturing environments, particularly in the medical device industry, and will utilize Lean and Six Sigma methodologies to drive efficiency. **

Job Summary

  • The Senior Industrial Engineer will lead and implement manufacturing systems and process improvements for electro-mechanical and robotic medical device assembly.
  • Johnson & Johnson provides an inclusive work environment that respects diversity and offers comprehensive benefits including retirement plans, paid time off, and parental leave.
  • This role requires strong application of Lean and Six Sigma methods, data-driven decision making, and alignment to medical device regulatory requirements to deliver robust and efficient production systems.

Matching Summary

Match Score: 75

** Johnson & Johnson is seeking a Senior Industrial Engineer to lead manufacturing systems and process improvements in Santa Clara, CA. The ideal candidate will have significant experience in regulated manufacturing environments, particularly in the medical device industry, and will utilize Lean and Six Sigma methodologies to drive efficiency. **

Salary

Base: $109,000.00 - $174,800.00; Bonus/Equity: Not specified; Benefits: Retirement plan, 401(k), vacation, sick time, parental leave, and other paid time off

Skills & Requirements

Must-have

  • Lean and Six Sigma methods
  • Process design and validation
  • Labor and capacity modeling
  • Value stream optimization
  • Line balancing and cost reduction
  • Manufacturing documentation compliance
  • Data-driven decision making

Nice-to-have

  • Coaching and mentoring junior engineers
  • Collaboration with IT/automation teams
  • Experience with CAD and simulation tools
  • Familiarity with medical device regulatory requirements
  • Integration of automation and robotics
  • Use of PLM/ERP/MES systems
  • Basic data scripting skills

Key Requirements

  • Bachelor’s degree in Industrial or related Engineering
  • 6+ years industrial/manufacturing engineering experience
  • Experience in regulated manufacturing environments
  • Lean and continuous improvement certification
  • Process validation expertise (IQ/OQ/PQ)
  • Six Sigma Green/Black Belt certification preferred
  • Ability to travel up to 15%

Work Rights

Not specified

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