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At Capstan Medical, we’re building one of the most exciting and innovative companies in medtechdeveloping 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 spacecreating the perfect place to do meaningful, career-defining work.
Reports to:Quality Manager
Workplace type:Onsite in Santa Cruz, CA
Manufacturingresponsibilities include:
Oversee product quality during all stages of productionandfield service.
Ensure compliance with Good Manufacturing Practices (GMP) regulations and internal quality management systems throughout the manufacturing process.
Lead and support investigations into nonconforming materials and products (NCRs), working closely with cross-functional teams including Manufacturing and Engineering,identifyingroot causes, ensuringtimelyresolution, and implementing effective corrective and preventive actions (CAPAs) to prevent recurrence.
Conduct Material Review Board andparticipatein materials decision making.
Establish, implement, and supportprocesses forfield serviceand reworkofroboticmedical devices.
Maintain Device History Records for robotic medical devices
Supportcreationof risk management files, including the development of Process FMEA
Lead and support process validation activities, including IQ/OQ/PQ (Installation Qualification/OperationalQualification/Performance Qualification), for new and existing manufacturing processes.
Develop validation protocols, execute validation activities, and compile validation reports to ensure process robustness and consistency.
Collaborate with cross-functional teams, including Manufacturing and Engineering, to resolve quality issues andidentifyopportunities for process improvement and efficiency gains within the manufacturing environment.
Perform audits of manufacturing processes, including inspections, testing, and documentation, toidentifyareas for improvement and ensure adherence to quality standards.
Implement Lean and Six Sigma principles to drive continuous improvement initiatives.
Testing responsibilities include:
Collaborate withcross-functionalteams to ensure thatdesign, manufacturing, and standards-based testrequirements are met.
Provide guidance on processes and validations to ensure product safety and compliance.
Packaging and Finished Goods Releaseresponsibilities include:
Oversee packaging validation activities to ensure product integrity and stability during storage and transportation.
Participate in finished goods release processes, ensuring compliance with release criteria and applicable regulatory requirements.
Documentation and Complianceresponsibilities include:
Maintainaccurateand up-to-date documentation related to quality control processes, inspection results, metrology records, nonconformance reports, and corrective actions.
Ensure compliance with relevant regulatory requirements, such as FDA QSR and ISO 13485 standards.
Support internal and external audits, including preparation of documentation, participation in audits, and implementation of audit findings.
Bachelor's degree in Engineeringora relatedtechnical field.Master'sdegree is a plus.
Minimum of5years of experience in a manufacturing quality engineering role within the medical device industrysupporting electromechanical capital devices.
In-depth knowledge of FDA regulations, ISO 13485,IEC 60601-1,and other relevant quality& safetystandards forroboticmedical devices.
Experience with nonconforming material investigations and implementing effective CAPAs.
Ability to work in a fast-paced environment
Experiencesupportingdevelopmentand manufacturing of surgical roboticdevices.
Certifications such as Six Sigma and ASQ Certified Quality Engineer (CQE) or Certified Quality Auditor (CQA).
Familiarity with process validation (IQ/OQ/PQ),electrical safety testing, and packaging requirements for medical devices.
Strong understanding of GMP regulations and quality management systems.
Excellent problem-solving skills and ability to apply root cause analysis methodologies.
Detail-oriented with effective organizational and documentation skills.
Strong communicationand collaboration skills to work cross-functionally and interact with technicians, engineers, auditors, and third parties.
Attention to detail, with a focus on accuracy and precision in quality-related activities.
We offer a fun, fast-paced, collaborative environment where you will be working ontransformationaltechnologiesin thecardiachealthcare space.
We offer outstanding benefits with medical, dental,and vision covered at 100% for you and your family, as well as flex time off.
Wethrive in ourwork-hard, play-hardenvironment. Bring your bike or running shoesifyou’dlike orjust be ready to enjoy a fun office outing.Weenjoytime 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.
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.