Manufacturing Engineer Ii - Shockwave

Johnson & Johnson UK

Santa Clara, California, United States
$73,000.00 to $117,300 annually; annual performanc...
Process/product improvement projects
Functional and destructive testing
Statistical analysis using minitab
The Manufacturing Engineer II is responsible for providing engineering support to Production, including designing, developing, testing, and implementing processes, tooling, and fixtures for commercial product

Job Summary

  • The Manufacturing Engineer II is responsible for providing engineering support to Production, including designing, developing, testing, and implementing processes, tooling, and fixtures for commercial product.
  • Key responsibilities include sustaining activities on the production line, identifying and participating in cost reduction improvement projects, and supporting new product introduction and scaling up.
  • The role requires a Bachelor's degree in engineering, 3-5 years of experience in a medical device environment, and knowledge of applicable Quality System requirements.

Matching Summary

The Manufacturing Engineer II is responsible for providing engineering support to Production, including designing, developing, testing, and implementing processes, tooling, and fixtures for commercial product.

Salary

$73,000.00 to $117,300 annually; Annual performance bonus; Medical, dental, vision, life insurance, disability, business accident insurance, group legal insurance, pension, 401(k), vacation, sick time, holiday pay, work/personal/family time

Skills & Requirements

Must-have

  • Process/product improvement projects
  • Functional and destructive testing
  • Statistical analysis using Minitab
  • New product introduction support
  • Process FMEAs and MPIs
  • Bill of Materials (BOMs) and Lot History Records (LHRs)
  • Quality System Requirements support

Nice-to-have

  • Lean and Six Sigma concepts
  • Basic understanding of Statistics
  • Work in a fast-paced environment
  • Operate as a team or independently
  • Flexibility to changing requirements

Key Requirements

  • Bachelor's degree in engineering
  • 3-5 years of experience in medical device
  • Experience with Validation of Medical Devices (IQ-OQ-PQ)
  • Ability to create and maintain Drawings in SolidWorks
  • Experience with MES and ERP (Oracle) preferred

Work Rights

Not specified

Tailored Resume

Cover Letter