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Process Engineer Medical Device Jobs in California

Medical Device R&D Engineer

San Jose, CA ยท On-site

$115K - $175K/yr

... medical device company. Roles and Responsibilities * Contribute to the design, development, testing ... Bills of Materials (BOMs) * manufacturing process instructions * engineering specifications * risk ...

Medical Device R&D Engineer

San Jose, CA ยท On-site

$115K - $175K/yr

... medical device company. Roles and Responsibilities * Contribute to the design, development, testing ... Bills of Materials (BOMs) * manufacturing process instructions * engineering specifications * risk ...

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 ...

Process Engineer

Lake Forest, CA ยท 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 ...

Process Engineer We are seeking a Process Engineer to support a pharmaceutical manufacturing ... Experience with syringe or disposable medical device manufacturing. * Cleanroom filling experience.

New

Process Engineer

Lake Forest, CA ยท 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 ...

Showing results 41-60

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 Aug 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 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 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 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.

Infographic showing various Process Engineer Medical Device job openings in California as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $90,813 per year, or $43.7 per hour.

Medical Device R&D Engineer

AngioSafe

San Jose, CA โ€ข On-site

$115K - $175K/yr

Full-time

Re-posted 14 days ago


Job description

AngioSafe is a Bay Area start-up focused on improving healthcare through state-of-the-art vascular interventional catheter device design, development, and manufacturing. We are pioneering the development of novel treatment mechanisms and algorithms to provide unprecedented access to peripheral and coronary disease treatments. Our experienced team is committed to developing and commercializing innovative, high-quality products that reduce risk and improve cardiovascular treatment outcomes. This onsite role will have a meaningful and direct impact on AngioSafe's device portfolio through the development of novel vascular interventional devices and support of existing product pipelines. The ideal candidate will combine strong engineering fundamentals with hands-on technical ability and thrive in a fast-paced startup environment.
Position Summary
We are seeking a highly motivated, hands-on Individual Contributor (IC) R&D Engineer to support the design, development, prototyping, testing, and manufacturing transfer of interventional catheter devices.This role is ideal for someone who enjoys building and testing devices directly, solving technical challenges, and working collaboratively within a small, rapidly evolving medical device company.
Roles and Responsibilities
  • Contribute to the design, development, testing, and manufacturing transfer of interventional catheter devices
  • Support development activities for both new and existing products
  • Perform hands-on prototyping, assembly, troubleshooting, and testing of medical devices
  • Generate technical documentation in accordance with Design Control requirements
  • Develop test methods, protocols, and reports for:
    • concept evaluations
    • verification & validation testing
    • component qualification
    • packaging and shelf-life validation
  • Support creation and maintenance of:
    • Bills of Materials (BOMs)
    • manufacturing process instructions
    • engineering specifications
    • risk management documentation
  • Work closely with suppliers to support component development and resolve non-conformance issues
  • Assist in maintaining shared laboratory and prototype spaces
  • Collaborate cross-functionally with engineering, manufacturing, quality, and leadership teams

Minimum Qualifications
  • Bachelor's degree in Mechanical Engineering or related engineering discipline preferred
  • Minimum 5 years of medical device R&D experience
  • Hands-on catheter prototyping and testing experience required
  • Experience working within ISO 13485 Design Controls required
  • Experience with document control systems and engineering change documentation
  • Strong hands-on engineering and troubleshooting abilities
  • Startup and/or small-company experience preferred
  • Proficiency with SolidWorks including:
    • 3D component and assembly modeling
    • 2D drawings per ASME Y14.5
  • Knowledge of catheter manufacturing materials and processes including:
    • braiding
    • lamination
    • laser welding
    • adhesive bonding
    • packaging
  • Strong communication and technical writing skills
  • Ability to manage multiple priorities in a fast-paced environment
  • Self-motivated with strong ownership mentality

Preferred Qualifications
  • Catheter design and development experience strongly preferred
  • Experience supporting FDA and/or Notified Body submissions
  • Experience using cloud-based document control systems
  • Project leadership experience preferred

Additional Information
  • This is a fully onsite role based in San Jose, CA
  • No relocation or immigration sponsorship available
  • Principals only please

Equal Opportunity Employer
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