Manufacturing Tech Iii

Johnson & Johnson

Santa Clara, California, United States of America
Base: $57,500.00 - $92,575.00; bonus/equity: annua...
Onsite
Electro-mechanical assembly
Iso 13485 and fda qsr compliance
Good documentation practices (gdp)
Johnson & Johnson is committed to healthcare innovation to prevent, treat, and cure complex diseases through smarter and less invasive treatments

Job Summary

  • Johnson & Johnson is committed to healthcare innovation to prevent, treat, and cure complex diseases through smarter and less invasive treatments.
  • The Manufacturing Technician III role involves advanced electro-mechanical assembly, testing, troubleshooting, and maintaining compliance with medical device regulations in a fast-paced production environment.
  • Employees benefit from competitive compensation, performance bonuses, comprehensive health and retirement plans, and various paid leave options.

Matching Summary

Johnson & Johnson is committed to healthcare innovation to prevent, treat, and cure complex diseases through smarter and less invasive treatments.

Salary

Base: $57,500.00 - $92,575.00; Bonus/Equity: Annual performance bonus eligible; Benefits: Medical, dental, vision, life insurance, disability, retirement plans, paid time off

Skills & Requirements

Must-have

  • Electro-mechanical assembly
  • ISO 13485 and FDA QSR compliance
  • Good Documentation Practices (GDP)
  • Electrical troubleshooting with multimeters
  • Use of precision assembly tools
  • Medical device clean manufacturing protocols
  • Production schedule adherence

Nice-to-have

  • Robotics and motion-control systems experience
  • Process validation knowledge (IQ/OQ/PQ)
  • Continuous improvement methodologies
  • Cross-functional collaboration skills
  • Independent work in fast-paced environment
  • Training and mentoring team members
  • Problem-solving and root cause investigation

Key Requirements

  • 4–5 years medical device manufacturing experience
  • Vocational Certificate, Technical, or Associate degree
  • Knowledge of GDP and GMP standards
  • Ability to work overtime and flexible shifts
  • Experience with ISO 13485 and FDA QSR
  • Strong mechanical and electrical troubleshooting skills

Work Rights

Not specified

Tailored Resume

Cover Letter