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R&D Market Engineer

Job in San Jose, Santa Clara County, California, 95199, USA
Listing for: PROCEPT BioRobotics
Full Time position
Listed on 2026-02-28
Job specializations:
  • Engineering
    Manufacturing Engineer, Mechanical Engineer, Product Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below
Position: Staff R&D  Market Engineer

Overview

Embark on an enriching journey with PROCEPT Bio Robotics, where our vision, mission, and values guide everything we do. We put the patient first in everything we do and are committed to revolutionizing treatment for benign prostatic hyperplasia (BPH) through innovation in surgical robotics. As our company grows, we aim to improve the quality of life for patients, provide more effective treatment options for surgeons, and uphold the trust of our shareholders.

We are focused on creating an evolving landscape for your career with transformative opportunities that provide continuous growth.

The Opportunity That Awaits You

This amazing opportunity in the R&D department puts you in charge of projects focused on market engineering for the robotic system. The work here makes a real difference to PROCEPT’s product cost and quality; it will require innovation, creativity, solid engineering skills, robust testing, and clear documentation. You will regularly collaborate with other organizations including quality, manufacturing, supply chain, regulatory, and the clinical groups.

Your work is critical in providing a safe, precise, and high-value product for our customers. You will be working with both internal engineering, failure analysis, production, and external teams such as commercial and field service.

What Your Day-To-Day Will Involve
  • Fully participate in and contribute to project teams including activities: product design and development, test of materials, preparation of specifications, process capability studies, research investigations (animal and clinical studies), report preparation, and process/test documentation
  • Work collaboratively with other engineers, quality, manufacturing, supply chain, regulatory, clinical, and marketing to ensure project success
  • Take a lead role for on-market engineering over designated assemblies of the robotic platform, focused on the handpiece and other disposables and accessories
  • Design, develop, and improve on-market medical device systems and support new product development as needed by the business
  • Generate engineering documentation including:
    Solid Works 3D models, 2D prints, product specifications, test protocols, test reports, dFMEA, HA, BOM, etc.
  • Design, procure, and fabricate tooling and fixtures for testing, development, and/or manufacturing
  • Read, analyze, and interpret general business periodicals, professional journals, procedures, or governmental regulations
  • Perform troubleshooting on new products/processes
  • Design and coordinate standard engineering tests, procedures, and experiments
  • Summarize, analyze, and draw conclusions from test results
  • Prepare standard reports/documentation to communicate results to the technical community
  • Interface with vendors for component sourcing and fabrication (machining, sheet metal, rapid prototyping, injection molding, MIM, weldments, PCB, etc.)
  • Independently manage projects and outside consultants, as needed
  • Maintain trained status for, and comply with, all relevant aspects of the PROCEPT Bio Robotics Quality Management System to ensure product quality and regulatory compliance
  • Understand and adhere to the PROCEPT Bio Robotics Quality and Environmental, Health & Safety policies
Qualifications We Need You to Possess
  • BS Mechanical Engineering (or similar engineering degree)
  • 8+ years of experience in the medical device industry
  • Proficiency using CAD (Solid Works) to design and document mechanisms, with strength in design analysis
  • Proven experience in mechanism design and electro-mechanical systems
  • Familiar with motion control, position sensing, feedback algorithms, motors, encoders, and linear actuators; experience with drivetrain components such as gear trains, lead screws, splines, cams, linear guides, belts, and pulleys
  • Understanding of component selection criteria, and design for reliability and manufacturability
  • Experience with designing products in an FDA or other regulated industry; comfortable with design input, design output, traceability, and risk analysis
  • Knowledge of component manufacturing processes (including machining, sheet metal, rapid prototyping, injection molding, MIM, weldments, PCB, etc.)
  • Comfortable with all phases…
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