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Capstan Medical, Inc.

Sr/Staff Manufacturing Engineer, Robot Productization

Santa Cruz, California, United States

Location
Santa Cruz, California, United States
Work
On-site
Employment
Full-time
Level
Lead / staff
Function
Engineering
Pay
Not stated
Posted
5 weeks ago

Pay and the market here

22 engineering jobs open in Santa Cruz: 5% remote, 2 posted in the last 30 days.

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About the role

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

Source

Posted by Capstan Medical, Inc. on their own hiring page, jobs.lever.co. OptiTalent shows it as published, read 07 Nov 2026 11:25 UTC; the original is the reference.

View the original ad ↗

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