Staff Mechanical Engineer, Advanced Product Development (Robotics)

Intuitive•Sunnyvale, CA

22h•$163,800 - $277,300•Onsite

About The Position

The Advanced Product Development group within Intuitive Surgical is searching for a hands-on engineer with a focus on the mechanical design of next generation surgical robot systems and robotic components, contributing to the exploration of new applications of surgical robotics. This role is an exciting opportunity to join a small and innovative team in the early phases of product development. The hands-on Staff Mechanical Engineer will conceptualize, develop, and verify new mechanical design concepts for next generation of minimally invasive surgical robot systems. The candidate will apply their product development expertise to next generation da Vinci designs, leveraging their creativity and engineering analysis to the design of kinematics, robotic actuation and sensing solutions. The candidate will have the technical depth to resolve complex mechanical, materials, and mechanical design issues. In addition, the candidate shall have the ability to work in an interdisciplinary team to analyze and provide solutions for both lower-level component and higher-level system issues. They must excel in a high-energy, focused, small-team environment, and have a commitment to high quality prototypes and concepts. They must demonstrate a track record of developing, creating, and innovative engineering solutions. A strong sense of shared responsibility and shared reward is required as well as a commitment to high product quality.

Requirements

Organizational skills and ability to manage deliverables under tight deadlines, set priorities, and manage time effectively.
Possess a strong mechanical aptitude and a finely honed intuition for electromechanical design
Familiarity with volume manufacturing processes which may include cast metal, injection molded plastic, sheet metal stamping, and others.
Self-driven to achieve individual and collaborative results in a high-energy, small, focused team environment, to maintain a strong sense of shared responsibility and shared reward, and to foster a positive and encouraging group culture.
Comfortable with ambiguity and able to build clarity and consensus among cross-functional stakeholders.
Strong understanding of material and component selection criteria as well as design for reliability and manufacturability best practices
Strong analytical and problem-solving skills such as FEA, statistical, and experimental design
Exemplary communication and documentation skills with the ability to clearly present to larger groups and distill complex information.
Experience interfacing with external suppliers, consultants, customers, and potential business partners.
Highly proficient in CAD design, drawing, and GD&T proficiency to design and document complex mechanisms and systems (SolidWorks preferred).
BS or MS in Mechatronics, Mechanical Engineering, Systems Engineering or related engineering or scientific discipline
Minimum 12 years designing mechanical engineering products or relevant experience (Robotics experience preferred)

Nice To Haves

Project management, planning, and change management skills. Able to manage multiple fast-paced projects simultaneously.
Experience with FDA QSR 21 CFR Part 820, ISO 13485, IEC 60601, and other related external standards.
Experience working in medical devices or similar regulated industries

Responsibilities

Design and develop the mechanical hardware of new robotic systems to meet performance, manufacturability, and reliability specifications, including design, documentation, and procurement of components and subassemblies.
Develop and implement design strategies for new products to meet target costs and performance requirements.
Lead multi-disciplinary technical teams on the design, requirements generation, documentation, pilot builds, and characterization for robotic joints and subsystems.
Create detailed mechanical assemblies and prototypes with consideration for performance, first principles thinking, cost, manufacturability and safety.
Development and documentation of mechanical design and manufacturing documentation including inspection procedures, assembly instructions, new manufacturing processes, test methods, purchase specifications, BOMs, component / assembly drawings per the company’s operating procedures.
Provide written protocols, reports, drawings, specifications, presentations, and perform technical design reviews to solicit feedback on design activities on an ongoing basis.
Contribute to budget, resource, and planning of technical projects and workstreams.
Create and maintain SolidWorks CAD databases, including assemblies, components, and detailed drawings.
Contribute to and make decisions based on risk assessments, industry standards, and regulatory frameworks.
Observe pre-clinical and clinical cases and interface with clinical experts to inform designs and identify user needs.
Document, prepare and review patent submissions.