ZipRecruiter

Log In

1

Process Engineer Medical Device Jobs in California

Astrix Inc

Medical Device Assembler

Santa Rosa, CA · On-site

$19.75 - $24/hr

Pay Rate Low: 22 | Pay Rate High: 26 The Medical Device Assembler is responsible for assembling ... Work with supervisors, engineers, and technicians to resolve line issues and support process ...

Intellectt INC

Senior Mechanical Engineer

San Jose, CA · On-site

$122K - $161K/yr

Senior Mechanical Engineer (Medical Device) Location: San Jose, CA Job Summary: Seeking an experienced Senior Mechanical Engineer with 10+ years in the medical device industry. Candidate must have ...

TEEMA

Lead Swift/iOS Medical Device SWE

San Diego, CA · On-site

$175K - $210K/yr

Lead iOS (Swift) Software Engineer - Medical Device Startup We're partnering with a well-funded, fast-growing startup to hire a Lead iOS/Swift Software Engineer. This is a high-impact, full-time role ...

next page

Showing results 1-20

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 Jun 13, 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 are the key skills and qualifications needed to thrive in the Process Engineer Medical Device position, and why are they important?

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 some common projects or responsibilities I might take on as a Process Engineer in the medical device industry?

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 is a Process Engineer Medical Device job?

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 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 June 2026, with employment types broken down into 80% Full Time, and 20% Contract. Highlights an 100% In-person job distribution, with an average salary of $90,813 per year, or $43.7 per hour.

Sustaining / Process Engineer Medical Device

AngioSafe

San Jose, CA • On-site

$120K - $160K/yr

Full-time

Posted 14 days ago

Job description

Role: Sustaining / Process Engineer Company: AngioSafe Location: San Jose, CA Position Type: Full-Time on site

Overview:

AngioSafe is a Bay Area start-up focusing on improving healthcare delivery through state-of-the-art catheter development. Our seasoned experts are committed to producing high quality and innovative products to decrease risk and improve outcomes of arterial disease.

We are seeking a Manufacturing/Process Engineer to support the production and improvement of our innovative catheters ensuring high reliability, regulatory adherence, and cost-effective manufacturability. This is a hands-on role requiring direct involvement with manufacturing equipment. Candidates with primarily theoretical or design-only backgrounds will not be a fit.

Roles and Responsibilities:

  • Primary focus: Support the manufacturing line and advance the processes and device in order to support scale up.
  • Create and document new manufacturing processes as necessary for production at significantly higher volumes and validate as appropriate
  • Support ongoing manufacturing activities including dealing with production equipment, non-conformances, facilities and other line related issues. This includes SOLVING issues with laminators, laser welders, hot boxes, etc.
  • Spending significant time on the manufacturing line alongside the assemblers to improve processes and increase quality. You are the primary interface between engineering and production.
  • Assist development of assembly and test fixturing with a focus on quality and volume
  • Write protocols & test reports related to validation activities
  • Collaborate with existing suppliers to improve manufacturability and decrease cost
  • Qualify components from new suppliers in order to improve supply chain flexibility

Skills, Experience, & Behaviors:

  • Solid history of experience in a medical device manufacturing environment (~5+ years preferred)
  • Hands-on mechanical aptitude with direct experience working on production equipment is required
  • Solid experience with either lamination or laser welding is required
  • Proficiency in SolidWorks is helpful but not required
  • Proven experience editing Manufacturing Procedures (MPs), Lot History Records (LHRs), Bills of Materials (BOMs), etc. is required
  • Comfort using inspection and test equipment (vision systems, tensile testing) is a plus
  • Experience working within and maintaining compliance in a highly regulated environment
  • Demonstrated ability to work independently in a fast-paced, small company environment
  • Flexibility and willingness to take on a variety of roles
  • Demonstrated ability to collaborate effectively, especially with a team of diverse assemblers
  • Strong verbal and written communication skills.

    No relocation or immigration support provided for this role.

    Principals only Please

    AngioSafe is committed to a diverse workplace and is committed to equal opportunity employment for all job applicants without regard to race, color, religion, sex, sexual orientation, age, gender, gender identity or expression, size, national origin, disability, or veteran status. AngioSafe complies with all applicable local, state, and national laws governing non-discrimination in employment.