Staff Manufacturing Engineer - Shockwave

Johnson & Johnson

Santa Clara, California, United States
Base: $105,000 to $169,050 annually; bonus/equity:...
Process development and implementation
Process failure modes and effects analyses
Dmaic methodology
The Staff Manufacturing Engineer is responsible for designing, developing, testing, documenting, and implementing processes, tooling, and fixtures for throughout the product lifecycle, from design to production

Job Summary

  • The Staff Manufacturing Engineer is responsible for designing, developing, testing, documenting, and implementing processes, tooling, and fixtures for throughout the product lifecycle, from design to production.
  • This role will work closely with production, quality, and R&D teams to support the company’s manufacturing operations and product launch timelines.
  • The anticipated base pay range for this position is $105,000 to $169,050 annually, with eligibility for an annual performance bonus and comprehensive benefits.

Matching Summary

The Staff Manufacturing Engineer is responsible for designing, developing, testing, documenting, and implementing processes, tooling, and fixtures for throughout the product lifecycle, from design to production.

Salary

Base: $105,000 to $169,050 annually; Bonus/Equity: Eligible for annual performance bonus; Benefits: Medical, dental, vision, life insurance, disability, retirement plan, savings plan, time off benefits

Skills & Requirements

Must-have

  • Process development and implementation
  • Process Failure Modes and Effects Analyses
  • DMAIC methodology
  • Process improvement projects
  • Product/process engineering problem solving
  • Cost reduction plans

Nice-to-have

  • Pioneering development and commercialization
  • Innovative healthcare solutions
  • Team player and independent operator
  • Adaptable to changing requirements

Key Requirements

  • Bachelor's degree in Mechanical or Biomedical Engineering
  • Minimum of eight (8) years of experience in a medical device environment
  • Knowledge of QSRs, FDA, ISO, MDD
  • Experience with Process Validations (IQ, OQ, PQ)
  • Experience applying statistics and using statistical software
  • Proficiency in Solidworks, Minitab
  • Ability to work in a fast-paced environment

Work Rights

Not specified

Tailored Resume

Cover Letter