Sr/Staff Manufacturing Engineer, Robot Productization

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Summary

Location

Santa Cruz, United States

Work

Full-time

Experience

7+ years

About this Job

There is no playbook for what we're building. Capstan is bringing a first-of-its-kind surgical robot to patients, and the processes to build it reliably at scale don't exist yet – you'll help create them. This isn't sustaining a mature product on a settled line. You'll join a newly formed team that works hand in hand with R&D owning the productization elements of the design.

In this role, you'll lead the productization of new robotic subsystems – from early engineering builds, through a series of pre-DV builds, to DV and clinical production. You'll develop the build and test processes, special processes, fixtures, and documentation that turn a design into a repeatable product, and you'll use each build to find and close gaps before they reach the line. You'll thrive here if you've brought complex electro-mechanical systems into production before, love being on the floor with the hardware, and want to shape how a novel robot is built from day one.

If you're a driver who seeks out issues, converges the team on solutions, and excels at pushing projects across the finish line in a growth-stage company, this is the role for you.

Key Responsibilities:

  • Lead the productization of new robotic subsystems, partnering with R&D from early engineering

builds through pre-DV, DV, and clinical builds

  • Own the path from design to product – drive open issues, decisions, and actions to closure

across R&D, Quality, Supply Chain, and Manufacturing, and escalate risks early to keep builds on schedule

  • Plan and drive build readiness for each development build – documentation, fixtures, materials,

equipment, line setup, and training – and use each build to find and close gaps before the next

  • Develop and characterize special processes (eg. adhesive bonding and curing, welding, press fits,

crimping), including surrogate testing and DOEs

  • Create and mature manufacturing documentation, including MPIs, DHRs, and in-process

inspection points, from redline drafts to released procedures

  • Design, qualify, and release assembly fixtures, tooling, and equipment, and define calibration

and preventive maintenance needs

  • Provide DFM/DFA feedback early in development, including error-proofing (poka-yoke) features,

to make designs easier to build, test, and service

  • Define line layout, process flow, cycle time, and staffing needs for new products, including

facility, utility, safety, and environmental requirements

  • Make make-vs-buy decisions for processes and partner with suppliers on outsourced processes

and critical components

  • Establish traceability and serialization for assemblies and components, and firmware/software

versions

  • Own process risk management (PFMEA) and drive process capability (Cpk) and process

validation plans with Quality

  • Partner with manufacturing software engineers to integrate test, calibration, and firmware

loading into the build flow

  • Lead troubleshooting and root cause investigations (5 Whys, Fishbone, DMAIC) on build issues

across mechanical, electrical, and software domains

  • Mentor engineers and technicians, and incorporate technician feedback into processes and

documentation

What you'll need:

  • Bachelor's or Master's degree in Mechanical Engineering, Manufacturing Engineering,
  • Mechatronics, Electrical Engineering, or related field
  • Minimum 7 years of manufacturing engineering experience for Senior, or 10+ years for Staff (a
  • Master's degree can offset years of experience)
  • Proven track record bringing complex electro-mechanical systems from development into
  • production (robotics, medical capital equipment, or similar)
  • Hands-on experience developing special processes (eg. bonding, welding, press fits, crimping)
  • Experience designing and qualifying fixtures and tooling using CAD (SolidWorks or similar)
  • Working knowledge of process controls and statistics (DOE, Cpk, Gage R&R) and process risk
  • tools (PFMEA)
  • Demonstrated success leading root cause investigations and implementing design and process
  • fixes
  • Experience working in a regulated environment (eg. ISO 13485, 21 CFR 820)
  • Excellent communication and documentation skills, and comfortable leading cross-functional
  • teams
  • Strong project leadership: able to plan, drive, and close cross-functional work without formal
  • authority
  • Hands-on, detail-oriented, and able to work independently in a fast-paced environment
  • Eagerness to learn and push the envelope to bring a novel surgical robotic platform to market

Preferred:

  • Experience in an early-stage company or on a first-generation product, standing up processes,
  • lines, and documentation from scratch
  • Mechatronics background: comfortable reading electro-mechanical schematics and debugging
  • integrated mechanical, electrical, and software systems
  • Experience with motors, encoders, brakes, sensors, and motion control assemblies
  • Scripting and data analysis skills (Python, MATLAB, or similar)
  • Experience with supplier qualification, outsourced special processes, and first article inspection
  • Familiarity with lean manufacturing principles and line design

About the Company

Capstan Medical, Inc. logo

Capstan Medical, Inc.

Privately Held
Robotics Hardware & ComponentsHealthcare & Life Sciences

At Capstan Medical, we’re driven by an unwavering commitment to transforming the treatment of structural heart disease. By merging surgical robotics with catheter-based technology and next generation implants, we’ve pioneered a patient-optimized approach to repair and replace heart valves.

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