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Process Engineer Medical Device Jobs in California

Talentry, LLC

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Sr. Mechanical Engineer - Medical Device

San Diego, CA · On-site

$130K - $180K/yr

Senior Mechanical Engineer - Medical Device San Diego, CA (Onsite) 130,000-180,000 DOE Join a growing medical-device team developing and improving a precision electromechanical product. This is an ...

UL Solutions

Staff Engineer - Medical Device

Brea, CA · On-site

$115K - $160K/yr

Resolves engineering issues associated with Variation Notices by analyzing and reporting on the ... This position also provides health benefits such as medical, dental and vision; wellness benefits ...

UL Solutions

Staff Engineer - Medical Device

Brea, CA · Hybrid

$115K - $160K/yr

Join our team, connect with global experts and help shape the next generation of medical technology. * University Degree in Electrical Engineering or related field. * 10+ years of Compliance ...

UL Solutions

Staff Engineer - Medical Device

Brea, CA · Hybrid

$115K - $160K/yr

Join our team, connect with global experts and help shape the next generation of medical technology. * University Degree in Electrical Engineering or related field. * 10+ years of Compliance ...

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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.

Manufacturing Engineer - Medical Device (Process

Stark Pharma Solutions Inc

Irvine, CA • On-site

$78K - $105K/yr

Contractor

Posted 2 days ago

New

Job description

ABOUT COMPANY:

Stark Pharma Solutions Inc is a life sciences staffing and consulting firm supporting pharmaceutical, biotechnology and medical device organizations across the United States. We place quality, validation, manufacturing and regulatory professionals with companies building and scaling FDA-regulated operations. Our clients range from established manufacturers to early-stage sites standing up their first quality systems.

Manufacturing Engineer – Medical Device (Process Validation, NPI, Lean)

JOB SUMMARY:

Our client, a medical device manufacturer, is seeking a Manufacturing Engineer to support production operations and process improvement on the manufacturing floor. The role covers process validation, tooling and fixture support, new product introduction and day-to-day troubleshooting in an ISO 13485 environment.

RESPONSIBILITIES:

  • Support daily production operations and troubleshoot process and equipment issues on the manufacturing floor
  • Execute process validation activities (IQ/OQ/PQ) for manufacturing equipment and processes
  • Drive process improvement initiatives to improve yield and reduce scrap and cycle time
  • Design and qualify tooling and fixtures to support production
  • Develop and update work instructions, routers and manufacturing documentation
  • Support new product introduction (NPI) and transfer to manufacturing
  • Process engineering change orders (ECO/ECN) and assess manufacturing impact
  • Support non-conformance and CAPA investigations related to manufacturing processes

QUALIFICATIONS:

  • Bachelor's degree in Mechanical, Industrial, Biomedical or Manufacturing Engineering
  • 3–5 years of manufacturing engineering experience in medical device
  • Experience with process validation (IQ/OQ/PQ)
  • Working knowledge of ISO 13485 and 21 CFR Part 820
  • CAD experience, SolidWorks preferred, and working knowledge of GD&T
  • Lean Manufacturing and Six Sigma exposure
  • Must be legally authorized to work in the United States
  • W2 employment only

HOW TO APPLY:

Please send your resume to deepika.b@starkpharma.com. In your email, please include your current location, your hourly rate expectation on W2, and your availability to start.