Senior Supplier Development Engineer – Plastics (medical Devices)

Johnson & Johnson

Irvine, California, United States
$94,000.00 - $151,800.00 py
On-site
Scientific injection molding
Injection molding tool design
Measurement system analysis
Johnson & Johnson is seeking a Senior Supplier Development Engineer specializing in plastics for its medical devices division in Irvine, California. The role focuses on engineering processes, project management, and compliance in the development of innovative vision treatments, requiring a strong background in engineering and experience with medical device manufacturing

Job Summary

  • An engineering professional who applies scientific knowledge, engineering knowledge, mathematics, and ingenuity to complete assignments related to a specific technical field or discipline.
  • Works with external manufacturers (EMs) to provide continuity of supply, failure investigations, and sustaining support.
  • Develops, writes, and executes validation protocols and reports.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking a Senior Supplier Development Engineer specializing in plastics for its medical devices division in Irvine, California. The role focuses on engineering processes, project management, and compliance in the development of innovative vision treatments, requiring a strong background in engineering and experience with medical device manufacturing.

Salary

$94,000.00 - $151,800.00

Skills & Requirements

Must-have

  • Scientific Injection Molding
  • Injection Molding Tool Design
  • Measurement System Analysis
  • Design of Experiments
  • Process Capability Analysis
  • Injection Molding Qualification
  • external and sub tier suppliers

Nice-to-have

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

Key Requirements

  • Bachelor's degree in engineering
  • Five years of engineering/operational experience
  • Plastics Engineering and Biomedical Engineering background
  • Medical device experience
  • Experience with External Manufacturers and Sub-Tier suppliers
  • Supplier component validations
  • IQ/OQ/PQ documentation

Work Rights

Not specified

Tailored Resume

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