Senior Mechanical Engineer – Medical Devices Innovator

Fortive

Irvine (CA)

On-site

USD 120,000 - 160,000

Full time

14 days+

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Job summary

Fortive in Irvine, CA is seeking a Sr Mechanical Engineer to plan and execute mechanical design and development for medical device systems and components. You will manage projects of moderate scope and collaborate cross-functionally to ensure quality and regulatory compliance.

Key activities include creating and validating 3D models and drawings with GD&T, developing test protocols, conducting design reviews, and documenting verification and validation.

Qualifications

  • Bachelor's degree in Mechanical Engineering or related field.
  • 10+ years of mechanical design experience in regulated industry (or 7+ years with Master's).
  • Proficient in SolidWorks and GD&T principles.

Responsibilities

  • Plan and conduct mechanical design for complex components and subsystems using advanced engineering principles.
  • Create and validate 3D models, drawings, and specifications in GD&T.
  • Develop and execute test protocols; analyze results and suggest improvements.
  • Lead design reviews and resolve complex issues.
  • Perform verification and validation testing documentation.
  • Prepare technical docs, proposals, and cost estimates for planning.
  • Collaborate across functions and with external partners to ensure timely delivery.
  • Apply FBS tools to optimize design processes and product quality.

Skills

SolidWorks
GD&T
Design for manufacturing
Problem solving
Communication
Electrical safety
Cross-functional coordination
MS Office

Education

Bachelor's degree in Mechanical Engineering

Tools

SolidWorks
Visio

Job description

Fortive in Irvine, CA is seeking a Sr Mechanical Engineer to plan and execute mechanical design and development for medical device systems and components. You will manage projects of moderate scope and collaborate cross-functionally to ensure quality and regulatory compliance.

Key activities include creating and validating 3D models and drawings with GD&T, developing test protocols, conducting design reviews, and documenting verification and validation.

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