Senior Supplier Development Engineer – Plastics (medical Devices)

Johnson & Johnson

Irvine, California, United States
$94,000.00 - $151,800.00; not specified; not speci...
**
Supplier development for plastics
Medical device manufacturing
Scientific injection molding
** Johnson & Johnson is seeking a Senior Supplier Development Engineer with a focus on plastics for their medical devices division in Irvine, California. The ideal candidate will have a strong engineering background, particularly in plastics and biomedical engineering, and experience with external suppliers in the medical device industry. **

Job Summary

  • Johnson & Johnson is committed to building a world where complex diseases are prevented, treated, and cured through healthcare innovation.
  • The Senior Development Engineer will drive functional performance ensuring the highest standards in quality, customer service, and regulatory compliance.
  • Employees are eligible for various benefits including a consolidated retirement plan, savings plan, long-term incentive program, and comprehensive time off benefits.

Matching Summary

Match Score: 75

** Johnson & Johnson is seeking a Senior Supplier Development Engineer with a focus on plastics for their medical devices division in Irvine, California. The ideal candidate will have a strong engineering background, particularly in plastics and biomedical engineering, and experience with external suppliers in the medical device industry. **

Salary

$94,000.00 - $151,800.00; Not specified; Not specified

Skills & Requirements

Must-have

  • Supplier development for plastics
  • Medical device manufacturing
  • Scientific Injection Molding
  • Injection Molding Tool Design
  • Measurement System Analysis
  • Design of Experiments
  • Process Capability Analysis

Nice-to-have

  • Agile Decision Making
  • Emerging Technologies
  • Lean Supply Chain Management
  • Technologically Savvy
  • Situational Awareness

Key Requirements

  • Bachelor's degree in engineering
  • Minimum five years engineering/operational experience
  • Experience with external and sub-tier suppliers
  • Medical device experience (21 CFR Part 820, ISO13485)
  • Supplier component validations
  • Processing technical documents (IQ/OQ/PQ)

Work Rights

Not specified

Tailored Resume

Cover Letter