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Intuitive Surgical

Builds robots for minimally invasive surgery

Senior NPI Manufacturing Engineer

Manufacturing EngineeringConfirmed live in the last 24 hours
Full-timeSunnyvale, CA, USAIn-person

About the Job

Requirements

  • Strong technical analytical and troubleshooting skills.
  • Prior responsibility for validation and verification of processes, equipment, and products.
  • Strong organizational skills and the ability to work on several fast-paced projects simultaneously.
  • Prior experience managing product and process changes.
  • Prior experience with technical writing.
  • Ability to communicate effectively and professionally with cross-functional peers, executive leadership, internal customers, and external suppliers.
  • Minimum Bachelor of Science degree in an Engineering discipline; a Master of Science degree is preferred.
  • Minimum 8 years of experience as a design or manufacturing engineer supporting products with significant mechanical, electromechanical, or electro-optical content.
  • Experience with ISO 13485, ISO 9001, or a medical device manufacturing environment; Six Sigma Black or Green Belt is a plus.
  • Experience with Design Control processes for medical devices, clinical applications of surgical instruments, or automated equipment design is a plus.
  • Fundamental understanding of engineering plastics, especially medical-grade polymers, and metals such as Nitinol, PTFE, Pebax, PET, and Nylon is a plus.
  • Familiarity with mechanical computer-aided design software such as SolidWorks is a plus.
  • Strong technical analytical skills and a background in material bonding, catheters, and vision-related products are a plus.
  • Background in material bonding, catheters, and vision-related products.
  • Familiarity with the fundamentals of injection molding.

Responsibilities

  • Develop new and improved manufacturing processes by collaborating across functions to solve technical process and equipment problems, including processes for flexible instruments and catheters such as lamination, thermal bonding, injection molding, and ultraviolet-cured adhesives.
  • Contribute to developing manufacturing processes, including early development of flexible instrument manufacturing processes and process tradeoff assessments.
  • Work with plastic and metal joining processes, including laser welding, adhesive bonding, lamination or plastic reflow, and injection molding.
  • Design experiments to identify and control critical process parameters, and transfer complex manual processes to high-volume, high-capability manufacturing.
  • Develop flexible instrument and catheter manufacturing lines by establishing operation sequences, building and testing prototypes, training operators, defining fixture and tooling requirements, and conducting process validation.
  • Maintain connections with catheter manufacturing equipment suppliers and stay informed about current processes and equipment.
  • Work upstream with product design engineers and represent manufacturing on product development teams.
  • Support Ion manufacturing lines by maintaining regular communication with production teams to address short- and long-term support needs.
  • Manage product reliability improvements from concept through implementation.
  • Identify, design, qualify, document, and introduce assembly and test fixtures and equipment.
  • Improve Ion instrument manufacturing process flows for manufacturability, reliability, efficiency, capacity, and safety.
  • Execute and mentor others in manufacturing process validations, process failure mode and effects analyses, and other elements of production Master Validation Plans.
  • Manage manufacturing strategy and production capability for Ion Instrument lines to minimize customer backorders.
  • Maintain compliance with the medical device quality system, including corrective action closure, discrepant material disposition, and Engineering Change Order implementation.
  • Provide technical support for failure analyses and root-cause investigations of product failures.
  • Contribute to group and individual objectives aligned with product development goals, including setting priorities and metrics and communicating progress.
  • Provide resource budget estimates for product and process improvements, tooling development, and testing.
  • Work with Quality and Regulatory teams to ensure compliance with appropriate Good Manufacturing Practice, design history file, and device history record guidelines under Food and Drug Administration requirements.

About the Company

Intuitive Surgical

Builds robots for minimally invasive surgery

Intuitive Surgical makes da Vinci robots that let surgeons operate through a few small incisions, and Ion, a robot that reaches deep into the lungs to take tissue samples. In 2000, da Vinci became the first robotic system cleared by the FDA for general laparoscopic surgery, meaning keyhole operations in the abdomen. A surgeon sits at a nearby console and steers robotic arms holding a 3D camera and wristed instruments, which turn hand movements into smaller, steadier motions. Hospitals buy or lease the robots, then keep paying for the instruments used in each operation and for service. Intuitive was founded in 1995 to commercialize robotic surgery research from SRI International and is based in Sunnyvale, California.

Company size
10,001+
Company stage
IPO
Headquarters
Sunnyvale, CA
Founded
1995

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