Quality Inspector I (2nd Shift)

Johnson & Johnson UK

Danvers, Massachusetts, United States of America
Base: $38,500.00 - $61,985.00; bonus/equity: not s...
Onsite
Perform inspections on purchased parts
Perform visual inspection under microscope
Perform mechanical inspection using advanced systems
The Quality Inspector I will perform inspections, checks, tests, review of quality documents such as a device history report and sampling procedures of incoming materials, parts/components, partially assembled or finished medical devices

Job Summary

  • The Quality Inspector I will perform inspections, checks, tests, review of quality documents such as a device history report and sampling procedures of incoming materials, parts/components, partially assembled or finished medical devices.
  • Perform visual inspection on large lots size under a microscope.
  • Perform mechanical inspection using advanced inspection systems including using a vision and or touch probe system.

Matching Summary

The Quality Inspector I will perform inspections, checks, tests, review of quality documents such as a device history report and sampling procedures of incoming materials, parts/components, partially assembled or finished medical devices.

Salary

Base: $38,500.00 - $61,985.00; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • Perform inspections on purchased parts
  • Perform visual inspection under microscope
  • Perform mechanical inspection using advanced systems
  • Perform electrical and optical cable testing
  • Accurately document inspection results
  • Maintain controlled document files
  • Monitor critical equipment and instrumentation

Nice-to-have

  • Ability to work in a cleanroom environment
  • Attention to detail
  • Ability to follow SOPs

Key Requirements

  • Prior experience in quality inspection/control or Medical Device preferred
  • Ability to read critical dimensions on component drawings
  • Knowledge in Geometric Dimensioning & Tolerance preferred
  • Knowledge in IPC – 610 preferred
  • Ability to use all standard inspection gages
  • Knowledge in ISO and GMP
  • US FDA 21 CFR QSR and ISO 13485 preferred
  • Ability to perform complex component inspection
  • Strong verbal and written English communication skills
  • Ability to execute tasks in a timely manner
  • Working knowledge of Microsoft Office Suite, MRP system
  • SAP knowledge desired
  • Receiving/logistics knowledge preferred

Work Rights

Not specified

Tailored Resume

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