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Process Engineer Medical Device Jobs in California

Astrix Inc

Medical Device Assembler

Santa Rosa, CA · On-site

$22 - $24/hr

Pay: $22-24/hour Position Summary The Medical Device Assembly Technician is responsible for ... Perform in-process quality inspections and provide timely feedback regarding quality or production ...

Applied Medical

Process Engineer

Lake Forest, CA · On-site

$71K - $80K/yr

Applied Medical is a new-generation medical device company with a proven business model and ... Position Description As a Process Engineer at Applied Medical, you'll lead cross-functional ...

Applied Medical

Process Engineer

Lake Forest, CA · On-site

$71K - $80K/yr

Applied Medical is a new-generation medical device company with a proven business model and ... Position Description As a Process Engineer at Applied Medical, you'll lead cross-functional ...

Applied Medical

Process Engineer

Lake Forest, CA · On-site

$71K/yr

Applied Medical is a new-generation medical device company with a proven business model and ... Position Description As a Process Engineer at Applied Medical, you'll lead cross-functional ...

Astrix Inc

Medical Device Assembler

Santa Rosa, CA · On-site

$21 - $24/hr

Perform in-process quality checks and identify quality or process issues. * Follow manufacturing ... Qualifications * 1+ year of manufacturing experience; medical device experience is a plus.

SlingShot Connections

Be Seen First

Medical Device Assembler

San Clemente, CA · On-site

$22.10/hr

Support engineering tests by executing defined test methods * Record and maintain documentation as ... Comfortable working in a regulated environment (medical device experience is a plus) * Ability to ...

BEPC INC

Be Seen First

Medical Device Assembler - 30531

Temecula, CA · On-site

$19.25 - $23.33/hr

Medical Device Assembler Location: Temecula, CA 92591 Employment Type: W2 Contract - 12 Months with ... technology, engineering, manufacturing, and project management. At BEPC, we are driven by ...

New

BEPC INC

Medical Device Assembler - 30531

Temecula, CA · On-site

$19.25 - $23.33/hr

Medical Device Assembler Location: Temecula, CA 92591 Employment Type: W2 Contract - 12 Months with ... technology, engineering, manufacturing, and project management. At BEPC, we are driven by ...

New

BEPC INC

Be Seen First

Medical Device Assembler - 30531

Temecula, CA · On-site

$19.25 - $23.33/hr

Medical Device Assembler Location: Temecula, CA 92591 Employment Type: W2 Contract - 12 Months with ... technology, engineering, manufacturing, and project management. At BEPC, we are driven by ...

New

SlingShot Connections

Medical Device Assembler

San Clemente, CA · On-site

$18.50 - $22.75/hr

Support engineering tests by executing defined test methods * Record and maintain documentation as ... Comfortable working in a regulated environment (medical device experience is a plus) * Ability to ...

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Showing results 41-60

All JobsProcess Engineer Medical Device JobsProcess Engineer Medical Device Jobs in California

Process Engineer Medical Device information

See California salary details

$48.9K

$90.8K

$140.6K

How much do process engineer medical device jobs pay per year?

As of Sep 7, 2026, the average yearly pay for process engineer medical device in California is $90,813.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,500.00 and $101,700.00 per year, depending on experience, location, and employer.

What is a process engineer medical device?

A Process Engineer in the medical device industry is responsible for designing, implementing, and optimizing manufacturing processes to ensure efficiency, quality, and compliance with regulatory standards. They work to improve production procedures, troubleshoot issues, and develop new process technologies. Their role involves collaborating with cross-functional teams, such as design, quality, and regulatory, to ensure medical devices meet industry requirements. Additionally, they analyze data, validate processes, and support continuous improvement initiatives to enhance product reliability and manufacturing scalability.

What does a process engineer medical device do?

As a Process Engineer in the medical device industry, you'll commonly work on projects such as optimizing manufacturing processes, implementing new technologies, and ensuring compliance with strict quality and regulatory standards. Your daily tasks may include designing and validating production methods, troubleshooting process issues, and collaborating closely with quality assurance, R&D, and production teams. You may also be involved in documentation, process scale-up for new products, and continuous improvement initiatives. The role is highly collaborative, requiring you to coordinate with both technical and non-technical staff to meet quality, efficiency, and regulatory goals.

What skills and qualifications are needed to thrive as a process engineer medical device?

A Process Engineer in Medical Devices typically requires a degree in engineering (such as chemical, biomedical, or mechanical engineering) and experience with manufacturing processes, quality systems, and regulatory compliance. Familiarity with tools like CAD software, statistical analysis programs, lean manufacturing techniques, and knowledge of standards such as ISO 13485 are common requirements. Strong problem-solving abilities, project management skills, and excellent communication facilitate successful interactions with cross-functional teams. These skills ensure efficient, high-quality, and compliant manufacturing processes critical to patient safety and company success.

What are popular job titles related to Process Engineer Medical Device jobs in California?

For Process Engineer Medical Device jobs in California, the most frequently searched job titles are:

What job categories do people searching Process Engineer Medical Device jobs in California look for?

The top searched job categories for Process Engineer Medical Device jobs in California are:

Process Engineer Medical Device jobs near you
Infographic showing various Process Engineer Medical Device job openings in California as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 16% Part Time, and 5% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $90,813 per year, or $43.7 per hour.

R&D Engineer (Medical Device)

Spirair, Inc.

South San Francisco, CA • On-site

$100K - $120K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 24 days ago

Key responsibilities

  • Design, develop, and validate new medical device concepts, materials, and processes to meet customer and manufacturability requirements.

  • Create detailed documentation and test protocols, perform verification testing, and modify designs to ensure functionality and market needs are met.

  • Collaborate with manufacturing, suppliers, and other disciplines to ensure product design for manufacturability and support product commercialization.

Job description

Spirair, a venture capital-backed medical device company, was co-founded by two Stanford Biodesign and Innovation fellows with a shared interest in optimizing outcomes and patient experience through innovation solutions. With a passion for developing elegant technologies that evolve care and enhance accessibility and effectiveness, the Spirair team is partnering with leading ENT advisors and industry veterans to offer treatment options that are both massively impactful and minimally invasive.

We are hiring an R&D Engineer who will be responsible for the design, development, and manufacturability of products in accordance with the Company's Quality Manual. This position will ensure that assigned products are designed to meet customer requirements as well as manufacturability requirements. Interact with other disciplines within the company to ensure appropriate process development and feedback. Direct interface with suppliers as well as customers (physicians) may be required. This is an excellent opportunity to join a growing startup company at an exciting time in its development.

Requirements

MAJOR DUTIES AND RESPONSIBILITIES

•Design and implement new methodologies, materials, machines, processes or products.

•Develop new concepts from initial design to market release.

•Ensure design control requirements are met, manage product development timelines and work with a cross functional team to bring new devices to commercialization in a timely fashion.

•Design test and assembly fixtures working with engineering and manufacturing as appropriate.

•Test designs to validate the ability to function as intended (including generating and reviewing test protocols) and offer design modifications to meet specific market needs.

•Participate in animal and cadaver feasibility studies as necessary throughout the development process to ensure desired functionality.

•Perform verification testing to establish that new devices meet design input specifications.

•Develop tools, if required, to accompany marketed device.

•Create detailed documentation throughout the various stages and steps in research and development.

•Work with manufacturing/production as required to ensure product manufacturability.

•Assume other duties as assigned or as determined to be appropriate to the company and/or position.

•May be required to provide technical support for regulatory/clinical or sales efforts.

•Actively participate and contribute to idea generation such as through brainstorming and IP development.

PREFERRED QUALIFICATIONS

Education and/or Job Experience:

•Bachelor’s degree in Engineering or equivalent.

•2-5 years of R&D experience.

Skills, Abilities, and Requirements:

•Proficiency in SolidWorks for solid models and dimensioned drawings.

•Good documentation skills.

•Ability to multi-task and prioritize with flexibility required in a start-up environment.

•Proficient in Microsoft Word/Excel/PowerPoint.

Benefits

Spirair offers highly competitive salaries and benefits, including medical, dental, and vision insurance, paid time off, and 401(k). Legal authorization to work in the US is required. We are not able to sponsor individuals for employment visas for this job. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment verification form upon hire.
We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

The expected base salary range for this role is $100,000 - $120,000. Compensation will be based on a variety of factors, including experience, qualifications and internal equity. This position is based in our South San Francisco, CA location.