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Medical Device System Engineer Jobs in California

Astrix Inc

Medical Device Assembler

Santa Rosa, CA · On-site

$22 - $24/hr

Pay Rate Low: 22 | Pay Rate High: 24 A medical device manufacturer is seeking a Production/Assembly ... Collaborate with supervisors, engineers, and technicians to resolve line issues and suggest ...

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 ... Operate and document work activities using an iPad and electronic manufacturing systems. * Maintain ...

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 ...

Marquee Staffing - OC

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Medical Device Packaging (Cleanroom)

Lake Forest, CA · On-site

$20 - $21/hr

Follow SOPs, work instructions, engineering drawings, and inspection procedures. * Maintain ... Medical device manufacturing experience preferred; 2+ years is highly desirable. * Experience in an ...

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 ...

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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 Sep 9, 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 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 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 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 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 September 2026, with employment types broken down into 1% As Needed, 62% Full Time, 32% Part Time, and 5% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $125,549 per year, or $60.4 per hour.

Software Medical Device Engineer

Pleasanton, CA • On-site

Stark Pharma Solutions Inc
See more jobs at Stark Pharma Solutions Incexternal

Contractor

Re-posted 13 days ago

Job description

Location: Pleasanton, CA .  

The contract is for 1 year.  

RESPONSIBILITIES:
• Plan and execute migration of requirements and related data from legacy tools (e.g., DOORS, Jama, Excel, Jira) into new platforms, ensuring data integrity, traceability, and compliance.
• Administer, configure, and maintain enterprise requirements management tools, including hierarchies, templates, workflows, versioning, and baselining in alignment with the quality system.
• Develop and maintain a requirements management plan in collaboration with cross‑functional teams, defining the overall requirements structure and links to associated design control documents.
• Create and maintain standardized requirements templates, traceability frameworks, and governance models based on quality and regulatory requirements.
• Maintain the requirements database, develop scripts or automation as needed, and support integrations or add‑in tools to improve usability and efficiency.
• Provide training, documentation, and ongoing support to engineers, serving as the primary functional expert for requirements tools and best practices.
REQUIRED QUALIFICATIONS:
• Bachelor’s degree in Engineering, Computer Science, Biomedical Engineering, or a related discipline for requirements management.
• A minimum of 5 years with hands on experience administering or configuring enterprise requirements management tools to support regulated development environments (e.g., Codebeamer, DOORS, Jama, or comparable platforms). Ability to quickly learn and adopt new tools is expected.
• Hands‑on experience with requirements migration from legacy tools.
• Strong understanding of medical device product development and design control principles.
• Excellent verbal and written communication skills, with the ability to train and support engineers at all levels.
• Ability to work effectively in a collaborative environment.
PREFERRED QUALIFICATIONS:
• Experience acting as a tool administrator, configuration owner, or advanced power user in a regulated development environment.
• Experience defining or scaling requirements management frameworks for large or multi‑team programs.
• Familiarity with medical device development (FDA 21 CFR Part 820) with the ability to configure tools to support compliant workflows.
• Experience supporting software‑driven, connected, or mobile medical devices.
• Experience with different requirements management or lifecycle tools is valued; strong foundational understanding of requirements structures and traceability is more important than experience with a specific platform.
Abbott’s Heart Failure division is seeking a Requirements Tools Engineer to support medical device development by enabling and maintaining enterprise requirements management infrastructure. The role focuses on administering, configuring, and optimizing requirements tools, migrating data from legacy systems (e.g., DOORS, Jama, Excel, Jira), and ensuring data integrity, traceability, and regulatory compliance. The engineer collaborates with cross functional teams to define scalable requirements structures, templates, workflows, versioning, and baselining aligned with quality systems. Responsibilities also include developing requirements management plans, maintaining databases, supporting integrations or automation, and acting as the functional expert through training and ongoing support. The role requires 5+ years of hands on experience with enterprise requirements tools in regulated environments, strong knowledge of medical device design controls, and excellent communication skills. Experience with FDA 21 CFR Part 820, large scale programs, and software driven medical devices is preferred.