Principal Regulatory Affairs Specialist

At Capstan Medical, we are driven by an unwavering commitment to transforming the treatment of heart valve disease. By merging surgical robotics with catheter-based technology and next generation implants, we have pioneered a patient-optimized approach to repair and replace heart valves. Our innovative technology offers a significantly less invasive alternative to traditional open-heart surgery while ensuring a precise and reliable placement of the heart valve implant. With these advancements, we may be able to provide patients with a solution to their heart valve disease while significantly reducing recovery time and minimizing the risk of complications. With a dedicated team of heart valve device experts and robotics engineers, we are fully committed to developing a comprehensive and transformative solution that will positively impact the lives of individuals affected by this condition. Capstan Medical is uniquely positioned in Santa Cruz, CA; this gives us access to the amazing technical talent of the Bay Area but in an environment that we feel is conducive to doing our best creative work. Our office is adjacent to large tracts of open space with bicycle trails straight from the office doors offering access to the hills and beaches of Wilder Ranch State Park for road/mountain bicycle riding, hiking, and surfing. Come join us and become part of a team revolutionizing heart valve treatment! Description We are seeking a Principal RA Specialist to support Regulatory activities for the Capstan mitral and/or tricuspid valve products. As the Principal RA Specialist, you will be responsible for supporting global strategies, assigned Regulatory submissions/projects/requirements in varying geographies, as assigned, and ensuring product compliance. The Principal RA Specialist also supports cross-functional team guidance through product changes and approval. The role is fast-paced and evolving, requiring excellent collaboration, organizational and project management skills.