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Catheter Engineer Jobs (NOW HIRING)

Penumbra

Manufacturing Engineer I - Catheter

Roseville, CA · On-site

$72K - $94K/yr

General Summary The mission of the Manufacturing Engineering group is to provide manufacturing technology and robust solutions that commercialize new products and that support continuous improvement ...

AngioSafe

Medical Device R&D Engineer

San Jose, CA

Hands-on catheter prototyping and testing experience required * Experience working within ISO 13485 ... Strong hands-on engineering and troubleshooting abilities * Startup and/or small-company experience ...

West-Tech Materials

Sales Engineer

San Jose, CA · On-site

We are looking for sales engineers based in the Northern California area with experience and a basic understanding of catheter design, manufacturing and assembly including plastic extrusion, braiding ...

West-Tech Materials

Sales Engineer

San Jose, CA · On-site

We are looking for sales engineers based in the Northern California area with experience and a basic understanding of catheter design, manufacturing and assembly including plastic extrusion, braiding ...

Imperative Care

Principal R&D Engineer, NPD

Campbell, CA · On-site

$189K - $213K/yr

Lead assigned technical projects in catheter engineering group to drive value improvement, line extensions, and commercial compliance with quality systems and global regulatory requirements.

AngioSafe

Senior Medical Device R&D Engineer

San Jose, CA · On-site

$150K - $225K/yr

Hands-on catheter prototyping and testing experience required * Strong hands-on engineering mindset ... with ability to independently prototype, build, troubleshoot, and iterate device concepts * Startup ...

AngioSafe

Senior Medical Device R&D Engineer

San Jose, CA · On-site

$150K - $225K/yr

Hands-on catheter prototyping and testing experience required * Strong hands-on engineering mindset ... with ability to independently prototype, build, troubleshoot, and iterate device concepts * Startup ...

AngioSafe

Medical Device R&D Engineer

San Jose, CA · On-site

$115K - $175K/yr

Hands-on catheter prototyping and testing experience required * Experience working within ISO 13485 ... Strong hands-on engineering and troubleshooting abilities * Startup and/or small-company experience ...

AngioSafe

Medical Device R&D Engineer

San Jose, CA · On-site

$115K - $175K/yr

Hands-on catheter prototyping and testing experience required * Experience working within ISO 13485 ... Strong hands-on engineering and troubleshooting abilities * Startup and/or small-company experience ...

CYNET SYSTEMS

Senior Manufacturing Engineer

Plymouth, MN · On-site

$65/hr

Responsible for leading manufacturing engineering activities focused on catheter manufacturing processes, yield improvement, process optimization, and new product introduction. * The role involves ...

Stark Pharma Solutions Inc

Senior R&D Engineer

Minneapolis, MN · On-site

$109.10K - $149.80K/yr

We are currently hiring for a Senior R&D Engineer opportunity with one of our medical device ... Experience in catheter and/or single-use medical device development * Strong understanding of ...

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How much do catheter engineer jobs pay per year?

As of May 31, 2026, the average yearly pay for catheter engineer in the United States is $101,300.00, according to ZipRecruiter salary data. Most workers in this role earn between $90,000.00 and $115,000.00 per year, depending on experience, location, and employer.

What is a Catheter Engineer job?

A Catheter Engineer designs, develops, and tests catheter-based medical devices used for diagnostics or treatment. They work with materials, prototyping, and manufacturing processes to ensure the catheter meets performance, safety, and regulatory standards. Their role often involves collaborating with cross-functional teams, including clinicians and regulatory experts, to refine designs and bring products to market.

What are the key skills and qualifications needed to thrive in the Catheter Engineer position, and why are they important?

Success as a Catheter Engineer requires a background in biomedical engineering, materials science, or a related field, with experience in medical device design and development. Familiarity with CAD software, prototyping tools, ISO regulations, and FDA submission processes is typically expected. Excellent problem-solving skills, attention to detail, and the ability to communicate effectively within cross-functional teams set outstanding candidates apart. These skills ensure safe, innovative, and compliant catheter products that meet patient and regulatory needs.

What are some typical daily responsibilities for a Catheter Engineer?

Catheter Engineers regularly work on designing, prototyping, and testing new catheter products, ensuring compliance with medical standards and regulatory requirements. They collaborate closely with R&D teams, physicians, and quality assurance to refine product performance and address challenges encountered during development. Daily tasks may also include analyzing feedback from clinical trials, troubleshooting manufacturing issues, and preparing documentation for regulatory filings. This role is dynamic and involves balancing technical innovation with patient safety and usability considerations.
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Catheter Engineer jobs near you
Infographic showing various Catheter Engineer job openings in the United States as of May 2026, with employment types broken down into 99% Full Time, and 1% Part Time. Highlights an 84% Physical, 5% Hybrid, and 11% Remote job distribution, with an average salary of $101,300 per year, or $48.7 per hour.
Manufacturing Engineer I - Catheter

Manufacturing Engineer I - Catheter

Penumbra

Roseville, CA • On-site

$72K - $94K/yr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 8 days ago

Penumbra rating

7.8

Company rating: 7.8 out of 10

Based on 28 frontline employees who took The Breakroom Quiz

Job description

General Summary
The mission of the Manufacturing Engineering group is to provide manufacturing technology and robust solutions that commercialize new products and that support continuous improvement in production.  Project opportunities are designed to develop professional work knowledge and abilities and to support the efforts and projects that have global importance to the success of the business.  Area of work involves manufacturing processes with interaction between production and cross-departmental engineering groups in resolving problems encountered on the production floor and across the business. Evaluates, selects, and applies exciting engineering techniques, procedures, and criteria, using judgment in developing and implementing adaptations and modifications on the production line and to quality systems.   
 
Specific Duties and Responsibilities
Solve problems and implement innovative solutions. *
Execute detailed root cause analysis and recommend vetted solutions. *
Communicate and explain problems and solutions cross-functionally and interdepartmentally. *
Approach problems from a detail-oriented perspective. *
Support production; Creating and maintaining product and process documentation; Monitor process and equipment performance and identify and implement process improvement activities to increase/optimize yield, efficiency, and/or throughput. *
Design fixtures, acquire off-the-shelf tooling and equipment, and implement new fixturing on the production line. Perform equipment qualifications. *
Test processes, equipment, raw materials, and product. Perform process validations. Author protocols to execute tests and write reports and make conclusions and/or recommendations based on test results *
Plan, schedule, conduct, and coordinate detailed phases of engineering work as part of a project or as a total project. *
Develop specifications of a product, process, or piece of equipment. *
Develop, characterize, and optimize processes using statistical techniques and engineering knowledge and experience. *
Coordinate with the appropriate suppliers and other external resources needed in developing and implementing process improvement plans. *
Participate in project planning and scheduling. *
Train assemblers, quality control and technicians, as necessary, on processes, equipment, and documentation. *
Adhere to the Company's Quality Management System (QMS) as well as domestic and global quality system regulations, standards, and procedures. * 
Understand relevant security, privacy and compliance principles and adhere to the regulations, standards, and procedures that are applicable to the Company. * 
Ensure other members of the department follow the QMS, regulations, standards, and procedures. * 
Perform other work-related duties as assigned.
 
*Indicates an essential function of the role
 
Position Qualifications
Minimum education and experience:  
Bachelor's degree in Mechanical, Biomedical, Electrical, Chemical, Materials, or Industrial Engineering or related degree, or an equivalent combination of education and experience
 
Additional qualifications:
1+ year relevant engineering experience preferred
Engineering experience in a manufacturing environment recommended, medical device industry preferred  
Excellent written, verbal and interpersonal communication skills required 
Knowledge of FDA regulations, Lean/Flow Manufacturing, and/or materials and manufacturing processes desired
Proficiency in Word, Excel, PowerPoint, Access and other computer applications required
 
Annual Base Salary: $72,000 to $94,000
Location: Roseville, CA 
 
Working Conditions
General office, laboratory, and clean room environments.
Willingness and ability to work on site. 
Potential exposure to blood-borne pathogens
Requires some lifting and moving of up to 25 pounds
Must be able to move between buildings and floors. 
Must be able to remain stationary and use a computer or other standard office equipment, such as a printer or copy machine, for an extensive period of time each day.  
Must be able to read, prepare emails, and produce documents and spreadsheets.   
Must be able to move within the office and access file cabinets or supplies, as needed. 
Must be able to communicate and exchange accurate information with employees at all levels on a daily basis.  
 
 
What We Offer
A collaborative teamwork environment where learning is constant, and performance is rewarded.
The opportunity to be part of the team that is revolutionizing the treatment of some of the world's most devastating diseases.
A generous benefits package for eligible employees that includes medical, dental, vision, life, AD&D, short and long-term disability insurance, 401(k) with employer match, paid parental leave, eleven paid company holidays per year, a minimum of fifteen days of accrued vacation per year, which increases with tenure, and paid sick time in compliance with applicable law(s).
 
Penumbra, Inc., headquartered in Alameda, California, is a global healthcare company focused on innovative therapies. Penumbra designs, develops, manufactures, and markets novel products and has a broad portfolio that addresses challenging medical conditions in markets with significant unmet need. Penumbra sells its products to hospitals and healthcare providers primarily through its direct sales organization in the United States, most of Europe, Canada, and Australia, and through distributors in select international markets. The Penumbra logo is a trademark of Penumbra, Inc.
 
Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, age, disability, military or veteran status, or any other characteristic protected by federal, state, or local laws.
 
If you reside in the State of California, please also refer to Penumbra's Privacy Notice for California Residents.
 
For additional information on Penumbra's commitment to being an equal opportunity employer, please see Penumbra's AAP Policy Statement.
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