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Medical Device System Engineer Jobs in California

AngioSafe

Medical Device R&D Engineer

San Jose, CA · On-site

$115K - $175K/yr

Minimum 5 years of medical device R&D experience * Hands-on catheter prototyping and testing ... Experience with document control systems and engineering change documentation * Strong hands-on ...

Infotech Spectrum

System Engineer

Sunnyvale, CA · On-site

System Engineer Location : Sunnyvale, CA (Need Locals) Duration : 6+ Months • Experience ... medical device hazard analysis and design of mitigations for risk highly desirable • Ability to ...

Astrix Inc

Medical Device Assembler

Santa Rosa, CA · On-site

$22 - $26/hr

Pay: $22-26/hour Position Summary The Medical Device Assembly Technician is responsible for ... Operate and document work activities using an iPad and electronic manufacturing systems. * Maintain ...

Aerotek

Medical Device Assembler

Irvine, CA

$19 - $23.25/hr

Clean Room Assembler / Medical Device Assembler This role focuses on assembling advanced medical ... The role involves frequent use of microscopes, including modern ergonomic systems designed to ...

VOLT

Medical Device Assembler

Irvine, CA · On-site

$18 - $19.75/hr

Follow standard operating procedures (SOPs) to ensure compliance with FDA, GMP, and quality system ... Prior experience as a Medical Device Assembler or Production Assembler preferred. * Previous ...

VOLT

Medical Device Assembler

Irvine, CA · On-site

$18 - $19.67/hr

Follow standard operating procedures (SOPs) to ensure compliance with FDA, GMP, and quality system ... Prior experience as a Medical Device Assembler or Production Assembler preferred. * Previous ...

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Showing results 21-40

All JobsMedical Device System Engineer JobsMedical Device System Engineer Jobs in California

Medical Device System Engineer information

See California salary details

$52.8K

$125.5K

$164.8K

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

As of Aug 16, 2026, the average yearly pay for medical device system engineer in California is $125,549.00, according to ZipRecruiter salary data. Most workers in this role earn between $96,700.00 and $154,900.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a medical device system engineer?

A Medical Device System Engineer requires a strong background in systems engineering, biomedical engineering, or a related field, along with expertise in medical device development and regulatory requirements. Familiarity with design tools (such as CAD and MATLAB), medical device quality standards (like ISO 13485), and risk management processes is highly valuable. Effective communication, problem-solving abilities, and teamwork distinguish candidates in collaborative, cross-disciplinary environments. These competencies are crucial for ensuring safe, innovative, and compliant medical devices that meet both user needs and regulatory expectations.

What are typical daily tasks and responsibilities for a medical device system engineer?

Medical Device System Engineers are often responsible for designing, testing, and integrating complex medical devices while ensuring adherence to regulatory standards and safety requirements. Their daily tasks can include drafting system architectures, collaborating with electrical, mechanical, and software teams, conducting risk analyses, reviewing technical documentation, and supporting troubleshooting efforts during product development. They also frequently attend cross-functional meetings to align project timelines and discuss design improvements. This role provides a dynamic balance of hands-on engineering, project management, and regulatory compliance, making it ideal for individuals who enjoy challenging, mission-driven work in healthcare technology.

What is a medical device system engineer?

A Medical Device System Engineer is responsible for designing, developing, and integrating complex medical device systems. They work across multiple engineering disciplines, including hardware, software, and regulatory compliance, to ensure that medical devices meet quality and safety standards. Their role involves risk analysis, system requirements definition, and verification and validation testing. They collaborate with cross-functional teams, including mechanical, electrical, and software engineers, as well as regulatory and clinical experts. Ultimately, they help bring safe and effective medical technologies to market.

What are the most commonly searched types of Medical Device System Engineer jobs in California?

The most popular types of Medical Device System Engineer jobs in California are:

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

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

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

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

Medical Device System Engineer jobs near you
Infographic showing various Medical Device System Engineer job openings in California as of August 2026, with employment types broken down into 63% Full Time, 6% Temporary, and 31% Contract. Highlights an 97% In-person, and 3% Hybrid job distribution, with an average salary of $125,549 per year, or $60.4 per hour.

Medical Device R&D Engineer

AngioSafe

San Jose, CA • On-site

$115K - $175K/yr

Full-time

Re-posted 4 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