Primary Function of Position:


  • The Product Engineering Test Engineer will help investigate performance, cost, and reliability improvements for Intuitive’s products, and complete the development, documentation, and execution of test protocols to evaluate these improvements. 

 

  • The successful candidate will have both the technical depth to understand complex electrical, mechanical, materials, and manufacturing design issues and the ability to work in an interdisciplinary team troubleshoot root cause higher-level system issues. 

 

  • A strong sense of shared responsibility and shared reward is required as well as a commitment thigh product quality.

Roles & Responsibilities:


  • Work in cross-functional project teams to develop and verify modifications surgical robots, instruments and accessories and related electro-mechanical subassemblies

 

  • Investigate and determine the root cause of both latent and emerging design, manufacturing or material defects

 

  • Develop, execute and document test plans and protocols for formal design verification and validation testing according to tcorporate standard and departmental operating procedures

 

  • Investigate clinical and functional requirements

 

  • Provide test engineering support for resolution of field and manufacturing issue

 

  • Ensure FDA/GMP and IScompliance through unit testing, peer reviews, and validation of hardware.

 

  • Support the CAPA and CPIP processes and quality/regulatory audits as required

 

  • Review appropriate manufacturing VRs and NCRs, or engineering changes (ECOs, MCOs, Deviations, etc.) that affect currently shipping products, assure that product quality is maintained or improved.

 

  • Establish individual goals consistent with overall project goals

Skill/Job Requirements:


  • Work in cross-functional project teams to develop and verify modifications surgical robots, instruments and accessories and related electro-mechanical subassemblies

 

  • Investigate and determine the root cause of both latent and emerging design, manufacturing or material defects

 

  • Develop, execute and document test plans and protocols for formal design verification and validation testing according to tcorporate standard and departmental operating procedures

 

  • Investigate clinical and functional requirements

 

  • Provide test engineering support for resolution of field and manufacturing issues

 

  • Ensure FDA/GMP and IScompliance through unit testing, peer reviews, and validation of hardware.

 

  • Support the CAPA and CPIP processes and quality/regulatory audits as required

 

  • Review appropriate manufacturing VRs and NCRs, or engineering changes (ECOs, MCOs, Deviations, etc.) that affect currently shipping products, assure that product quality is maintained or improved.

 

  • Establish individual goals consistent with overall project goals




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