Senior Mechanical Engineer - Robotic Surgery Systems

Intuitive Surgical, Inc.

Sunnyvale (CA)

In loco

USD 163.000 - 234.000

Tempo pieno

2 giorni fa
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Curriculum e lettera di presentazione personalizzati, pronti da inviare.

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Descrizione del lavoro

Intuitive Surgical, Inc. seeks a Mechanical Engineer to develop, document, and validate new robotic instrument designs for surgical applications. The role focuses on miniaturization, novel architectures, and ensuring manufacturability for high-volume production.

You will collaborate with multi-disciplinary teams, perform design reviews, run analyses, and contribute to design history files in line with FDA requirements.

Competenze

  • BSME with 8+ years experience or MSME with 6+ years, or PhD with 3+ years (preferred).
  • Experience across product development lifecycle including design, debugging, verification, qualification, implementation and transfer.
  • Strong analytical aptitude and fundamentals in mechanics.
  • Proficiency with 3D CAD tools and Finite Element Analysis.
  • Experience with high-volume manufacturing concepts and DFMEA.

Mansioni

  • Design, document and validate new product designs for robotic surgical instruments.
  • Miniaturize architectures to meet clinical needs.
  • Create architectures expanding tool sets from soft tissue to hard anatomy.
  • Conduct empirical validation and simulations on designs.
  • Develop fixtures for verification and validation testing.
  • Collaborate with suppliers to optimize DF/M manufacturing.

Conoscenze

3D CAD design
SolidWorks
Matlab
FEM/FEA
Prototyping
Python
C++
Design for manufacturability

Formazione

BSME with 8+ years; MSME 6+ years; PhD 3+ years
PHD preferred

Strumenti

Ansys/Pro Mechanica
Python
C++

Descrizione del lavoro

Intuitive Surgical, Inc. seeks a Mechanical Engineer to develop, document, and validate new robotic instrument designs for surgical applications. The role focuses on miniaturization, novel architectures, and ensuring manufacturability for high-volume production.

You will collaborate with multi-disciplinary teams, perform design reviews, run analyses, and contribute to design history files in line with FDA requirements.

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