Staff Manufacturing Engineer - Shockwave

Johnson & Johnson MedTech

Santa Clara, California, United States
Base: $105,000 to $169,050 annually; bonus/equity:...
Not specified
Process development and manufacturing
Statistical analysis and doe planning
Lean manufacturing and 6s experience
Johnson & Johnson MedTech is seeking a Staff Manufacturing Engineer for their Santa Clara, California location to support the development and commercialization of innovative medical device solutions. The ideal candidate will have a strong background in manufacturing engineering within a medical device environment, focusing on process design, validation, and collaboration with cross-functional teams

Job Summary

  • Johnson & Johnson is pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease.
  • The Staff Manufacturing Engineer will work closely with production, quality, and R&D teams to support manufacturing operations and product launch timelines.
  • Employees may be eligible for competitive compensation, performance bonuses, and comprehensive benefits including medical, dental, vision, retirement plans, and paid time off.

Matching Summary

Match Score: 85

Johnson & Johnson MedTech is seeking a Staff Manufacturing Engineer for their Santa Clara, California location to support the development and commercialization of innovative medical device solutions. The ideal candidate will have a strong background in manufacturing engineering within a medical device environment, focusing on process design, validation, and collaboration with cross-functional teams.

Salary

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

Skills & Requirements

Must-have

  • Process development and manufacturing
  • Statistical analysis and DOE planning
  • Lean Manufacturing and 6S experience
  • Use of Solidworks and Minitab software
  • Process Failure Modes and Effects Analyses (pFMEAs)
  • Cross-functional collaboration with R&D and QA

Nice-to-have

  • Ability to manage multiple priorities
  • Strong verbal and written communication skills
  • Problem solving using DMAIC methodology
  • Experience with supplier selection and development
  • Cost reduction and productivity analysis

Key Requirements

  • Bachelor’s degree in Mechanical or Biomedical Engineering
  • Minimum eight years medical device experience or six with Master’s degree
  • Knowledge of QSRs, FDA, ISO, MDD regulations
  • Experience with Process Validations (IQ, OQ, PQ)
  • Ability to lift up to 25 lbs occasionally

Work Rights

Not specified

Tailored Resume

Cover Letter