Production Engineering Co-op — Lean Six Sigma in MedTech

Johnson Johnson

Danvers (MA)

On-site

USD 40,000 - 50,000

Full time

5 days ago
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Job summary

Johnson & Johnson is seeking a Production Engineering Co-op to join the Danvers, MA team. You will help design, develop, and validate manufacturing processes, tooling, and fixtures, working with Operations, Product Development, and Quality Assurance.

The role emphasizes Lean/Six Sigma methods, process documentation, and compliance with GMP/ISO standards, with opportunities to learn in a global medical device environment.

Qualifications

  • Pursuing an engineering degree (Junior, Senior, or graduate student).
  • Prior work experience is desired; medical device experience is preferred.
  • Knowledge of Lean, Six Sigma, Kaizen, and continuous improvement methods; Green Belt preferred.
  • Ability to communicate ideas clearly, both verbally and in writing.
  • Working knowledge of SAP is desired.

Responsibilities

  • Support design, development, improvement, and validation of manufacturing processes, tooling, and fixtures.
  • Contribute to daily production needs, defect reduction, productivity improvements, and product quality with cross-functional teams.
  • Use Lean and Six Sigma tools to analyze process trends and identify optimization opportunities.
  • Support production of new products and changes in coordination with Operations, Product Development, and Quality Assurance.
  • Maintain compliance with GMP, GDP, FDA QSR, and ISO standards while documenting processes.

Skills

Lean
Six Sigma
Kaizen
Green Belt
Microsoft Office
SAP
Communication skills

Education

Engineering degree (pursuing)

Tools

Microsoft Excel

Job description

Johnson & Johnson is seeking a Production Engineering Co-op to join the Danvers, MA team. You will help design, develop, and validate manufacturing processes, tooling, and fixtures, working with Operations, Product Development, and Quality Assurance.

The role emphasizes Lean/Six Sigma methods, process documentation, and compliance with GMP/ISO standards, with opportunities to learn in a global medical device environment.

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