Manufacturing Assembler II

Jupiter Endovascular, Inc.; Menlo Park (CA); On-site; USD 41,000 - 48,000; Full time

Benefits offered by this job

Competitive pay + incentives

Equity opportunities

Top-tier health coverage

401(k) with employer contributions

Paid time off & holidays

Team lunches & events

Job summary

Jupiter Endovascular, Inc. in Menlo Park, CA, is seeking a Manufacturing Assembler to join the Vertex PE System team, assembling complex catheter-based medical devices in a regulated cleanroom.

This role demands advanced technical assembly skills, GMP awareness, and a commitment to quality and patient safety. The ideal candidate has hands-on experience with catheter manufacturing processes such as coil winding, braiding, hydrophilic coating, lamination, and bonding.

Qualifications

• 2+ years in medical device assembly, preferably catheter manufacturing.
• Strong understanding of GMP/FDA/ISO regulations in medical device manufacturing.
• Ability to read and interpret assembly drawings and instructions.
• Exceptional manual dexterity; able to operate small tools under a microscope.

Responsibilities

• Precisely assemble catheters and other medical devices following instructions and quality standards.
• Perform assembly tasks using hand tools, microscopes, and specialized equipment (bonding, sealing, lamination).
• Conduct in-process inspections and functional tests to ensure specifications are met.
• Document inspection results, lot traceability, and production data per SOPs and regulations.
• Participate in productivity, process, and quality improvement activities.
• Collaborate with engineering and quality teams to improve procedures and equipment.
• Support validation of new assembly methods and tooling.
• Diagnose and resolve minor assembly and equipment issues to minimize downtime.
• Work with other assemblers to meet team quality and productivity targets.
• Coordinate with engineering to maintain and calibrate equipment and tools.

Skills

Manual dexterity

Medical device assembly

GMP compliance

Reading drawings

Microscope operation

Education

High school diploma

Tools

Bonding equipment

Lamination tools

Measuring devices

Job description

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 Manufacturing Assembler is a key contributor to the Vertex PE System manufacturing team, responsible for assembling complex, high‑quality catheter‑based medical devices within a regulated cleanroom environment. This role requires advanced technical assembly expertise, a strong understanding of medical device manufacturing standards, and an unwavering commitment to quality, compliance, and patient safety.

This position will support daily production by operating precision tools and equipment, adhering to Good Manufacturing Practices (GMP), and ensuring all work meets regulatory and quality system requirements. This role offers a meaningful opportunity to directly impact patient outcomes by improving manufacturing efficiency, strengthening product quality, and promoting a culture of continuous improvement and workplace safety.

The ideal candidate brings hands‑on experience with advanced catheter manufacturing processes, including coil winding and/or braiding, hydrophilic coating, lamination and adhesive bonding. Success in this role requires the ability to perform reliably in a fast‑paced, start‑up manufacturing environment, with the flexibility to cross‑train across multiple processes as production needs evolve. Strong collaboration skills are also essential.

This is an in‑office role.

Responsibilities

• Precisely assemble catheters and other medical devices following detailed work instructions and established quality standards.
• Perform intricate assembly tasks using various hand tools, microscopes, and specialized equipment (such as bonding, sealing, and lamination tools).
• Perform in‑process inspections and functional testing to guarantee components and finished products comply with all specifications.
• Accurately document inspection results, lot traceability, and production data according to company SOPs and regulatory requirements.
• Actively participate in productivity, process, and quality improvement activities.
• Collaborate with engineering and quality teams to suggest and implement enhancements to assembly procedures and equipment.
• Support validation processes for new assembly methods and tooling.
• Diagnose and resolve minor assembly and equipment issues to minimize downtime.
• Work closely with other manufacturing assemblers to achieve team quality and productivity targets.
• Partner with engineering to ensure all equipment and tools are correctly maintained, calibrated, and fit for use.

Qualifications

• High school diploma or equivalent required
• Proven experience, typically, 2+ years in medical device assembly required, preferably with catheter manufacturing.
• Strong understanding of GMP, FDA, and ISO regulations in a medical device manufacturing environment. Adherence to strict hygiene and gowning protocols is required.
• Ability to read and interpret assembly drawings, work instructions, and technical manuals.
• Exceptional manual dexterity and ability to operate small hand tools, measurement devices, computer equipment, to include working with small components under a microscope.

Additional Requirements

• Overtime and weekend work may be required depending on production needs.
• The role may involve exposure to chemicals used in the manufacturing process.
• Ability to perform repetitive tasks with hands and fingers.
• Able to lift, carry, push and pull items up to 40lbs.
• Ability to perform tasks that require standing and walking for long periods of time up to the entire shift.
• Ability to work well under pressure and to meet multiple and occasional competing deadlines while maintaining a cooperative working relationship with other people.
• Ability to work in a highly detailed environment where mental focus and accuracy of work output is essential.
• Good organizational, oral and written communication skills, including ability to represent the Company to both internal and external audiences (Audit)
• Must have adequate vision (corrective lenses permitted) to read schematics, blueprints, or technical documentation.
• Must be comfortable donning PPE including safety glasses, shoes, gloves, lab coats, or other PPE as needed.

Why Jupiter Endovascular?

• Work in a culture built on shared purpose, where passionate teammates support one another and stay motivated by improving patient lives.
• Thrive in a collaborative environment that values new ideas, gives everyone a voice, and offers professional growth and exposure across departments as the company enters an exciting phase of expansion.
• Earn competitive pay with performance incentives and equity opportunities.
• Enjoy comprehensive, top of the market medical, dental, and vision coverage focused on meaningful premium support and smart savings.
• Access meaningful benefits including a top tier 401(k) with a best in‑class plan design which includes strong employer contributions, short and long‑term disability, life insurance, commuter benefits, and wellness support.
• Take advantage of a healthy paid time off policy, company holidays, and an environment that encourages a healthy work‑life balance.
• Strengthen relationships through shared experiences - from daily company‑provided lunches and Thursday socials to monthly potlucks, company events, and volunteer opportunities that have a real impact in the community.

Compensation: Our job titles may span more than one career level. The starting base pay for this role is between $30-$35. The actual base pay is dependent upon many factors, such as training, transferable skills, work experience, business needs, and location. The base pay range is subject to change and may be modified in the future. This role may also be eligible for equity, benefits, and 401(k) with matching.
Jupiter Endovascular provides equal employment opportunities to all applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

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As set forth in Jupiter Endovascular’s Equal Employment Opportunity policy,we do not discriminate on the basis of any protected group status under any applicable law.

If you believe you belong to any of the categories of protected veterans listed below, please indicate by making the appropriate selection.As a government contractor subject to the Vietnam Era Veterans Readjustment Assistance Act (VEVRAA), we request this information in order to measurethe effectiveness of the outreach and positive recruitment efforts we undertake pursuant to VEVRAA. Classification of protected categoriesis as follows:

A \"disabled veteran\" is one of the following: a veteran of the U.S. military, ground, naval or air service who is entitled to compensation (or who but for the receipt of military retired pay would be entitled to compensation) under laws administered by the Secretary of Veterans Affairs; or a person who was discharged or released from active duty because of a service‑connected disability.

A \"recently separated veteran\" means any veteran during the three‑year period beginning on the date of such veteran's discharge or release from active duty in the U.S. military, ground, naval, or air service.

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An \"Armed forces service medal veteran\" means a veteran who, while serving on active duty in the U.S. military, ground, naval, or air service, participated in a United States military operation for which an Armed Forces service medal was awarded pursuant to Executive Order 12985.