Sustaining Engineer II

Company

Summary:

Join a team that’s redefining what’s possible in cardiovascular treatment. At Jupiter Endovascular, we’re revolutionizing catheter-based therapies by bringing the precision and control of surgery to minimally invasive procedures. For decades, catheters have remained largely unchanged—rigid, unstable, and difficult to maneuver through the body’s winding anatomy. We’ve developed a transforming fixation technology that navigates flexibly through the vascular system, then locks into place to deliver treatment with surgical‑like stability and control.

Our device solves one of the longest‑standing challenges in endovascular procedures, empowering physicians and improving outcomes for millions of patients living with cardiovascular disease. We’re entering an exciting new phase—scaling up production, expanding our team, and preparing for commercial launch.

Founded and headquartered in Menlo Park, California, Jupiter Endovascular is led by a proven team of medical device entrepreneurs and backed by top‑tier investors across venture capital, private equity, and strategic partners. We’ve built a fast‑paced, collaborative culture grounded in innovation, teamwork, and purpose. Every role at Jupiter directly contributes to our mission: saving lives by advancing the future of endovascular therapy.

Position Overview: The Sustaining Engineer II will be a critical team member within the Product Development team at Jupiter with a focus on supporting ongoing design, process and quality improvements, supplier development, and supplier capacity expansions for Class II single‑use sterile catheter‑based products. The Sustaining Engineer II will be supporting component non‑conformances, root cause analysis, testing, qualification and supplier capacity ramp up for critical components, sub‑assemblies and processes related to the pulmonary embolectomy aspiration system in support of full commercial launch.

This individual will work cross‑functionally with Quality, Manufacturing, and Operations within an FDA regulated medical device environment. This position reports directly to an Engineering Manager.

The ideal candidate would act with passion and intensity in a medical device start‑up that is fast‑paced and collaborative and would display the ability to perform the requirements outlined below. For the right person, this position will be a tremendously exciting and career‑defining opportunity, making core contributions to a new paradigm of catheter‑based interventions.

This is an in‑office role.

• Continuous improvement of products, processes and suppliers.
• Lead and execute implementation of sustaining projects following change controls procedures.
• Manage internal and external communication for sustaining projects.
• Perform verification and validation testing as required to implement changes.
• Collaborate with Operations and Product Development to identify supply chain risks.
• Perform root cause analysis investigations of component failures and non‑conformances.
• Collaborate with suppliers and internal teams to implement corrective actions.
• Support resolution of customer complaint investigations related to component issues.
• Perform statistical analysis of data and recommend supplier corrective actions based on process monitoring and statistical process controls.
• Collaborate with Quality and Product Development to define component inspection requirements.
• Collaborate with Product Development to recommend improvements to next generation products and processes based on RCA investigations.
• Support supplier development, qualification, and capacity scale up to meet forecasted demand.
• Collaborate with suppliers to create and execute validation plans.
• Identify, develop and qualify new suppliers as required to mitigate supply chain risks.
• Create and maintain QMS documentation related to sustaining projects.
• Recommend improvements to SOPs and work processes.
• Work effectively within the confines of a regulated, quality system driven, FDA monitored medical device environment.

• Required minimum education:
  
  Bachelor’s degree in engineering or related field
• Required minimum experience: 3 years in a related role
• Medical…