Capstan Medical
Sr/Staff Manufacturing Engineer, Robot Productization
Skills
24 days ago
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Important information
Contract type:
Permanent
Location:
Santa Cruz, CA, USA
Work mode:
Onsite
Published on:
1 October 2026
What they need
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
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