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Medical Device Engineer Jobs in California (NOW HIRING)

Bausch+Lomb Companies Inc.

$65K - $100K/yr

The Medical Device Engineer II supports the design and development of contact lenses within Bausch + Lomb's Vision Care R&D organization. This role serves as a product advocate on cross-functional ...

Intel

Device Engineer

Santa Clara, CA

$85K - $110K/yr

You will work closely with a team of engineers to push the boundaries of device performance, power ... Candidates should never be required to pay recruitment fees, medical examination fees, or any other ...

Murata America

Staff Device Engineer

San Mateo, CA · On-site

$260K/yr

Provide mentorship and technical guidance to engineers working on device modeling, characterization ... Comprehensive benefits package including medical, dental, and vision insurance. * Generous Paid ...

Murata Americas

Staff Device Engineer

San Mateo, CA · On-site

$260K/yr

Provide mentorship and technical guidance to engineers working on device modeling, characterization ... Comprehensive benefits package including medical, dental, and vision insurance. * Generous Paid ...

SlingShot Connections

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Medical Device Assembler

San Clemente, CA · On-site

$22.10/hr

Support engineering tests by executing defined test methods * Record and maintain documentation as ... Comfortable working in a regulated environment (medical device experience is a plus) * Ability to ...

AstrixTechnology LLC

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Medical Device Assembler

Santa Rosa, CA · On-site

$20 - $25/hr

Medical Device Assembler * Shift: Monday-Thursday, 5:00 AM - 3:30 PM (4/10 schedule) * Pay: $22-25/hour Position Summary The Medical Device Assembly Technician is responsible for assembling high ...

Astrix Inc

Medical Device Assembler

Santa Rosa, CA · On-site

$22 - $26/hr

Pay Rate Low: 22 | Pay Rate High: 26 Medical Device Assembler * Shift: Monday-Thursday, 5:00 AM - 3:30 PM (4/10 schedule) * Pay: $22-26/hour Position Summary The Medical Device Assembly Technician is ...

Aerotek

Medical Device Assembler

Irvine, CA · On-site

$19 - $23.25/hr

Clean Room Assembler / Medical Device Assembler This role focuses on assembling advanced medical devices, including urinary catheters and printed circuit board assemblies, in a clean room environment ...

Alarm.com

Senior Device Engineer

San Diego, CA

$126K - $167K/yr

We are looking for a talented and passionate embedded software engineer for the Device Engineering ... COMPANY BENEFITS Alarm.com offers competitive pay and benefits inclusive of subsidized medical plan ...

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Medical Device Engineer information

See California salary details

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How much do medical device engineer jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for medical device engineer in California is $49.18, according to ZipRecruiter salary data. Most workers in this role earn between $34.62 and $58.85 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a medical device engineer, and why are they important?

To thrive as a Medical Device Engineer, you need a solid background in biomedical, mechanical, or electrical engineering, often supported by a relevant bachelor's or master's degree. Familiarity with CAD software, regulatory standards (such as FDA or ISO 13485), and design validation tools is typically required. Strong problem-solving, communication, and teamwork skills are essential for collaborating on multidisciplinary projects and ensuring product safety. These competencies are crucial for developing innovative, compliant devices that improve patient outcomes and meet rigorous industry standards.

What does a medical device engineer do?

A Medical Device Engineer is responsible for designing, developing, testing, and improving medical devices used in healthcare settings. They work closely with doctors, scientists, and regulatory bodies to ensure that devices are safe, effective, and compliant with industry standards. Their work includes creating prototypes, conducting risk assessments, and overseeing the manufacturing process. Medical Device Engineers play a crucial role in bringing innovative technologies to market that help diagnose, treat, or monitor medical conditions.

What are some common challenges medical device engineers face when bringing a new product from concept to market?

Medical Device Engineers often encounter challenges such as navigating complex regulatory requirements, ensuring product safety and efficacy, and coordinating with cross-functional teams including design, manufacturing, and quality assurance. Balancing innovation with compliance, managing timelines, and addressing unforeseen technical issues are also typical hurdles. Successful engineers leverage strong project management and communication skills to collaborate effectively and bring devices to market efficiently.

What is the difference between Medical Device Engineer vs Biomedical Engineer?

AspectMedical Device EngineerBiomedical Engineer
CredentialsBachelor's or Master's in Engineering, certifications in medical device designBachelor's or Master's in Biomedical Engineering or related field
Work EnvironmentDesign, develop, test medical devices in labs or manufacturing settingsResearch, develop medical equipment, or work in clinical settings
Industry UsagePrimarily in medical device manufacturing companiesHospitals, research institutions, medical device companies

Medical Device Engineers focus on designing and testing specific medical devices, ensuring compliance and safety. Biomedical Engineers have a broader scope, working on medical equipment, implants, and research. Both roles require similar credentials and often overlap in industry settings, but their primary focus differs.

What does a medical device engineer do?

A medical device engineer is an engineering professional who develops new medical equipment and medical devices. As a medical device engineer, your work will vary depending on your area of expertise and may include biomedical research, material research and sourcing, computer-aided design work, and teaming up with doctors and patients. You also must understand the manufacturing process and ensure the products you design are both useful and cost-effective. You look for innovative solutions to medical problems and design new equipment diagnoses and treatments.

More about Medical Device Engineer jobs
What are the most commonly searched types of Medical Device Engineer jobs in California? The most popular types of Medical Device Engineer jobs in California are:
What are popular job titles related to Medical Device Engineer jobs in California? For Medical Device Engineer jobs in California, the most frequently searched job titles are:
What job categories do people searching Medical Device Engineer jobs in California look for? The top searched job categories for Medical Device Engineer jobs in California are:
What cities in California are hiring for Medical Device Engineer jobs? Cities in California with the most Medical Device Engineer job openings:
What are popular job titles related to Medical Device Engineer jobs in CA? For Medical Device Engineer jobs in CA, the most frequently searched job titles are:
Medical Device Engineer jobs near you
Infographic showing various Medical Device Engineer job openings in California as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $102,304 per year, or $49.2 per hour.

Software Medical Device Engineer

Stark Pharma Solutions Inc

Pleasanton, CA • On-site

Contractor

Re-posted 12 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.