DFX: collaborate with R&D to optimize parts for manufacturability and reliability.
Design/docs: create/refine CAD models, drawings, and tolerance analyses.
Inspection: develop inspection protocols and metrology methods.
Manufacturing partnerships: develop fixtures/tooling and CTQ controls.
Risk management: lead dFMEA and pFMEA to mitigate design/process risks.
Failure analysis: drive investigations to resolve design/material/process issues.

🎯 Requirements

Bachelor's degree in Mechanical Engineering or similar.
7+ years in medical device product development.
5+ years using SolidWorks.
Hands-on engineering orientation.
Experience with mechanical components, adhesives, PCBs, and cables.
Knowledge of design controls, risk management, and regulatory compliance for medical devices.

🎁 Benefits

Stock options.
Comprehensive benefits package.
401(k) program with matching contributions.

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