Quick overview
Job description
At Capstan Medical, we’re building one of the most exciting and innovative companies in medtech—developing a first-of-its-kind robotic platform for minimally invasive heart valve treatment. Our team combines surgical robotics, catheter-based delivery, and next-generation implants to transform complex procedures into safer, lower-stress solutions for patients and clinicians alike. As a highly collaborative, hands-on team, we move fast, wear multiple hats, and believe the best ideas can come from anyone.
Based in Santa Cruz, our unique workspace blends cutting-edge Bay Area innovation with a lifestyle-driven environment near trails, beaches, and open space—creating the perfect place to do meaningful, career-defining work.
Reports to: Quality Manager
Workplace type: Onsite in Santa Cruz, CA. (We are not considering candidates outside of California at this time. )
Description:
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Perform in-line inspections of surgical robotic components in accordance with approved procedures and specifications
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Conduct product label and packaging inspections to verify accuracy and compliance with approved procedures and requirements
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Inspect returned devices and document findings in accordance with established processes
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Review quality records such as Device History Records (DHRs) for completeness, accuracy, and compliance
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Identify and document nonconforming materials or processes; initiate Nonconformance Reports (NCRs) as required
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Quarantine and control movement of nonconforming material.
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Support investigation and resolution of quality issues in collaboration with Manufacturing and Engineering teams
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Represent Quality Assurance on the manufacturing floor and provide real-time quality guidance
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Maintain accurate inspection records and ensure timely data entry into quality systems
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Adhere to safety procedures and Good Manufacturing Practices (GMP)
Skills:
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Familiarity with inspection tools and techniques, including visual and dimensional inspection
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Working knowledge of quality systems, documentation practices, and GMP requirements
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Strong attention to detail and ability to follow written procedures
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Effective communication and teamwork skills
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Basic computer proficiency, including experience with electronic quality systems and Microsoft Office
Requirements:
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Excellent verbal and written communication skills.
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AA degree or equivalent directly transferable work experience
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Minimum of 3 years of professional experience working in quality inspection or manufacturing within the medical device industry. Preference for experience working with surgical robotic or other electromechanical devices.
Why join us:
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We offer a fun, fast-paced, collaborative environment where you will be working on transformational technologies in the cardiac healthcare space.
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We offer outstanding benefits with medical, dental, and vision covered at 100% for you and your family, as well as flex time off.
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We thrive in our work-hard, play-hard environment. Bring your bike or running shoes if you’d like or just be ready to enjoy a fun office outing. We enjoy time inside the office and out!
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