Quality Inspector I (2nd Shift)

Johnson & Johnson Innovative Medicine

Danvers, Massachusetts, United States of America
$38,500.00 - $61,985.00 py
Onsite
Perform inspections on purchased parts
Visual inspection under a microscope
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.
  • You will be responsible for performing inspections on multiple and varied purchased parts, subassemblies or finished product according to well-defined criteria using standard visual, physical, mechanical, and/or electrical measurements.
  • Employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)) and the Company’s long-term incentive program.

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

$38,500.00 - $61,985.00

Skills & Requirements

Must-have

  • Perform inspections on purchased parts
  • Visual inspection under a microscope
  • Mechanical inspection using advanced systems
  • Electrical and optical cable testing
  • Document inspection results accurately
  • Maintain controlled document files
  • Data entry into associated data systems
  • Monitor critical equipment and instrumentation
  • Identify problems and recommend corrective action

Nice-to-have

  • Work in a cleanroom environment
  • Knowledge in Geometric Dimensioning & Tolerance
  • Knowledge in IPC – 610
  • Receiving/logistics knowledge

Key Requirements

  • Prior experience in quality inspection/control or Medical Device preferred
  • Ability to read critical dimensions on component drawings
  • Ability to use all standard inspection gages
  • Knowledge in ISO and GMP
  • US FDA 21 CFR QSR and ISO 13485 preferred
  • Attention to detail with ability to follow SOPs
  • Ability to perform complex component inspection
  • Strong verbal and written English communication skills
  • Ability to execute tasks in a timely manner
  • Strong computer literacy required
  • Working knowledge of Microsoft Office Suite
  • MRP system; SAP knowledge desired

Work Rights

Not specified

Tailored Resume

Cover Letter