What are the responsibilities and job description for the IQC Quality Assurance Technician position at Capstan Medical?
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.
The IQC Quality Assurance Technician is responsible for inspecting incoming medical device components and materials to ensure they meet quality standards and regulatory requirements. This role supports incoming quality control activities, performs visual and dimensional inspections, reviews quality documentation, assists with nonconformance investigations, and helps maintain accurate quality records in a Class III medical device manufacturing environment. The technician works closely with Quality and Manufacturing teams to ensure the safety, reliability, and compliance of implantable medical devices and related equipment.
Responsibilities
Provide support in incoming Quality inspections for implantable medical device and/or capital equipment
Ability to perform visual inspections (i.e. detect defects) using a microscope and/or magnification visual inspection systems, calipers, etc.
High School graduate; AA degree is a plus
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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.
The IQC Quality Assurance Technician is responsible for inspecting incoming medical device components and materials to ensure they meet quality standards and regulatory requirements. This role supports incoming quality control activities, performs visual and dimensional inspections, reviews quality documentation, assists with nonconformance investigations, and helps maintain accurate quality records in a Class III medical device manufacturing environment. The technician works closely with Quality and Manufacturing teams to ensure the safety, reliability, and compliance of implantable medical devices and related equipment.
Responsibilities
Provide support in incoming Quality inspections for implantable medical device and/or capital equipment
- Provide support in execution of inspection and/or test procedures to evaluate all aspects of development of new products
- Provide support in review of Quality records such as Device History Records of product sub-assemblies and/or finished goods
- Provide support in Quality inspections of supplied medical device components and associated record keeping
- Assist Quality Assurance team in remedial actions to support disposition of product or component non-conformance
- Assist in environmental monitoring processes and associated record keeping
- Operate specialized equipment that supports established test and/or cleaning activities
Ability to perform visual inspections (i.e. detect defects) using a microscope and/or magnification visual inspection systems, calipers, etc.
- Ability to read manufacturing prints and identify associated specifications/characteristics related to inspection and testing to be performed
- Ability to use computer and general office software for data entry
High School graduate; AA degree is a plus
- 2-3 years of experience working in a Class III medical device manufacturing environment is preferred
- DHR (Device History Record) review experience is a plus
- Experience with structural implant heart devices is preferred
- We offer a fun, fast-paced, collaborative environment where you will be working on transformational technologies in the cardiac healthcare space that can make a meaningful impact for patients
- 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 may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.