Job Description

Work Flexibility: Onsite

What you will do

In this role, you will support Engineering initiatives that drive operational excellence within a regulated medical device reprocessing environment. You will contribute to increasing production capacity, optimizing manufacturing processes, improving safety, and enabling the successful introduction of new equipment and technologies, while ensuring compliance with regulatory and quality standards.

Main responsibilities:

  • Support the introduction of new manufacturing processes using Statistical, Lean, Good Manufacturing Practice (GMP), and Six Sigma methodologies.
  • Validate new equipment (including automated equipment) and manufacturing processes for production floor implementation.
  • Analyze process performance, conduct failure analyses, and implement improvements to enhance functionality and manufacturing efficiency.
  • Reduce scrap and reject rates through process optimization and ...

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