Quality Inspector Ii (2nd Shift)

Johnson & Johnson

Danvers, Massachusetts, United States of America
Base: $45,100.00 - $73,370.00; bonus/equity: not s...
Onsite
Perform visual and mechanical inspections
Read critical dimensions on drawings
Document inspection results accurately
Johnson & Johnson is seeking a Quality Inspector II for the 2nd shift in Danvers, Massachusetts, to ensure the quality of medical devices through inspections and documentation. The ideal candidate should have experience in quality control, especially in the medical device industry, with a strong attention to detail and technical skills

Job Summary

  • The Quality Inspector II will perform inspections, checks, tests, and review of quality documents for incoming materials and finished medical devices.
  • Employees are eligible for comprehensive benefits including 120 hours of vacation time, 480 hours of parental leave, and 13 days of holiday pay per calendar year.
  • The role requires strong attention to detail and the ability to execute tasks under general supervision while maintaining controlled document files.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking a Quality Inspector II for the 2nd shift in Danvers, Massachusetts, to ensure the quality of medical devices through inspections and documentation. The ideal candidate should have experience in quality control, especially in the medical device industry, with a strong attention to detail and technical skills.

Salary

Base: $45,100.00 - $73,370.00; Bonus/Equity: Not specified; Benefits: Vacation, Sick time, Holiday pay, Parental Leave, Bereavement Leave

Skills & Requirements

Must-have

  • Perform visual and mechanical inspections
  • Read critical dimensions on drawings
  • Document inspection results accurately
  • Use standard inspection gages and microscopes
  • Follow SOPs and quality procedures

Nice-to-have

  • Knowledge of Geometric Dimensioning & Tolerance
  • Familiarity with IPC-610 standards
  • Experience with SAP or MRP systems
  • Receiving and logistics knowledge
  • Ability to work in cleanroom environment

Key Requirements

  • Prior experience in quality inspection or control preferred
  • Knowledge of ISO and GMP regulations
  • US FDA 21 CFR QSR and ISO 13485 preferred
  • Strong computer literacy required
  • Ability to read technical data sheets

Work Rights

Not specified

Tailored Resume

Cover Letter