Staff Supplier Engineer, Plastics

Johnson & Johnson

Santa Clara, California, United States of America
Base: $118,000.00 - $203,550.00; bonus/equity: not...
Plastics component manufacturing processes
Supplier manufacturing process scale-up
Cross-functional team collaboration
Johnson & Johnson is committed to building innovative healthcare solutions that prevent, treat, and cure complex diseases while respecting diversity and providing an inclusive work environment

Job Summary

  • Johnson & Johnson is committed to building innovative healthcare solutions that prevent, treat, and cure complex diseases while respecting diversity and providing an inclusive work environment.
  • The Staff Supplier Engineer will lead the development and scale-up of plastics manufacturing processes for new product development and sustaining production within the Robotics and Digital Solutions franchise.
  • Employees are eligible for comprehensive benefits including retirement plans, long-term incentives, various types of leave, and a supportive interview process accommodating applicants with disabilities.

Matching Summary

Johnson & Johnson is committed to building innovative healthcare solutions that prevent, treat, and cure complex diseases while respecting diversity and providing an inclusive work environment.

Salary

Base: $118,000.00 - $203,550.00; Bonus/Equity: Not specified; Benefits: Retirement plans, long-term incentives, paid leave

Skills & Requirements

Must-have

  • plastics component manufacturing processes
  • supplier manufacturing process scale-up
  • cross-functional team collaboration
  • manufacturing process validation
  • root cause analysis and corrective actions
  • regulatory compliance for medical devices

Nice-to-have

  • mechatronics and robotics experience
  • Six Sigma and Lean methodologies
  • supplier qualification and process improvement
  • knowledge of GD&T
  • experience with statistical process control
  • mentoring junior engineers

Key Requirements

  • BS degree in Engineering or similar
  • minimum seven years regulated industry experience
  • knowledge of plastic manufacturing processes
  • understanding of 21 CFR part 820 and ISO 13485
  • up to 25% domestic and international travel
  • experience in medical device industry preferred

Work Rights

Not specified

Tailored Resume

Cover Letter