Staff 3d Process Engineer

Johnson & Johnson

Raynham, Massachusetts, United States of America
Base: $94,000.00 - $151,800.00; bonus/equity: not ...
Additive manufacturing process expertise
Process validation iq oq pq
Capa and quality management
The Staff Process Engineer provides engineering support for manufacturing operations within the Additive Manufacturing value stream, driving key business priorities including Health, Safety & Environment, Quality, Supply Chain performance, and Cost Management

Job Summary

  • The Staff Process Engineer provides engineering support for manufacturing operations within the Additive Manufacturing value stream, driving key business priorities including Health, Safety & Environment, Quality, Supply Chain performance, and Cost Management.
  • This role involves leading process development, validation, continuous improvement initiatives, and collaborating closely with cross-functional teams and suppliers to ensure scalable, robust, and compliant manufacturing processes.
  • Johnson & Johnson offers comprehensive benefits including retirement plans, long-term incentives, and various paid time off options such as vacation, sick leave, parental leave, and volunteer leave.

Matching Summary

The Staff Process Engineer provides engineering support for manufacturing operations within the Additive Manufacturing value stream, driving key business priorities including Health, Safety & Environment, Quality, Supply Chain performance, and Cost Management.

Salary

Base: $94,000.00 - $151,800.00; Bonus/Equity: Not specified; Benefits: Retirement plans, long-term incentives, paid time off

Skills & Requirements

Must-have

  • Additive Manufacturing process expertise
  • Process validation IQ OQ PQ
  • CAPA and quality management
  • Cross-functional team collaboration
  • Root cause analysis and problem solving
  • New Product Introduction support
  • Process stability and continuous improvement

Nice-to-have

  • Six Sigma or Lean certification
  • CAD/CAM proficiency
  • Project management experience
  • Mentoring and coaching skills
  • Knowledge of regulatory medical device requirements
  • Calibration and maintenance collaboration

Key Requirements

  • Bachelor’s degree or equivalent
  • Minimum 4 years professional experience
  • Experience leading IQ OQ PQ validation
  • Proven CAPA and quality system management
  • Strong structured problem solving skills
  • Experience supporting NPI and scale-up
  • Up to 15% travel availability

Work Rights

Not specified

Tailored Resume

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