Geared toward candidates with medical device industry experience comfortable with in-line robotic component inspections.
Derived from job-description analysis by Serendipath's career intelligence engine.
Original posting from Capstan Medical, Inc. via Lever
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::
Perform in-line inspections of surgical robotic components in accordance with approved procedures and specifications
Conduct product label and packaging inspections to verify accuracy and compliance with approved procedures and requirements
Inspect returned devices and document findings in accordance with established processes
Review quality records such as Device History Records (DHRs) for completeness, accuracy, and compliance
Identify and document nonconforming materials or processes; initiate Nonconformance Reports (NCRs) as required
Quarantine and control movement of nonconforming material.
Support investigation and resolution of quality issues in collaboration with Manufacturing and Engineering teams
Represent Quality Assurance on the manufacturing floor and provide real-time quality guidance
Maintain accurate inspection records and ensure timely data entry into quality systems
Adhere to safety procedures and Good Manufacturing Practices (GMP)
Skills::
Familiarity with inspection tools and techniques, including visual and dimensional inspection
Working knowledge of quality systems, documentation practices, and GMP requirements
Strong attention to detail and ability to follow written procedures
Effective communication and teamwork skills
Basic computer proficiency, including experience with electronic quality systems and Microsoft Office
Requirements::
Excellent verbal and written communication skills.
AA degree or equivalent directly transferable work experience
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::
We offer a fun, fast-paced, collaborative environment where you will be working on transformational technologies in the cardiac healthcare space.
We offer outstanding benefits with medical, dental, and vision covered at 100% for you and your family, as well as flex time off.
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!
We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, sex, sexual orientation, gender identity, veteran status, and disability, or other legally protected status.