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Medical Device Embedded System Engineer Jobs in Rancho Cucamonga, CA

Sapsol Technologies Inc

Golang Developer

Brea, CA · On-site

AWS Greengrass and IoT Core Engineer with Golang. Experience : Relevant experience of 10+ Years ... Collaborate with embedded systems teams to ensure seamless integration with hardware. Implement ...

Sapsol Technologies Inc

Golang Developer

Brea, CA · On-site

... embedded systems teams to ensure seamless integration with hardware. • Implement secure ... manage device authentication and authorization. • Monitor and troubleshoot IoT device fleets ...

Esri

System Engineer- ArcGIS

Redlands, CA · On-site

$120K - $197K/yr

You will be part of a talented cross-functional team of dynamic and passionate engineers to deliver ... medical, dental, vision, basic and supplemental life insurance for employees (and their families ...

Banks Power

Embedded Firmware Architect

Azusa, CA

Your expertise in embedded systems, communication protocols, and firmware development will be ... Provide technical guidance and mentorship to developers and engineers * Define and develop modular ...

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All JobsMedical Device Embedded System Engineer JobsMedical Device Embedded System Engineer Jobs in Rancho Cucamonga, CA

Medical Device Embedded System Engineer information

See Rancho Cucamonga, CA salary details

$63.9K

$140.3K

$196.2K

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

As of Aug 11, 2026, the average yearly pay for medical device embedded system engineer in Rancho Cucamonga, CA is $140,282.00, according to ZipRecruiter salary data. Most workers in this role earn between $113,900.00 and $167,100.00 per year, depending on experience, location, and employer.

What does a medical device embedded system engineer do?

A Medical Device Embedded System Engineer designs, develops, and maintains the embedded software and hardware used in medical devices such as pacemakers, infusion pumps, and diagnostic equipment. They ensure that the systems meet strict safety, reliability, and regulatory standards required in the healthcare industry. Their work involves programming microcontrollers, integrating sensors and communication modules, and collaborating with cross-functional teams to ensure the final product is safe, effective, and compliant with medical regulations.

How does a medical device embedded system engineer typically collaborate with cross-functional teams during product development?

As a Medical Device Embedded System Engineer, you’ll work closely with teams such as hardware engineers, software developers, quality assurance, regulatory affairs, and clinical experts. Collaboration is essential to ensure the embedded system meets safety, performance, and regulatory requirements. This often involves participating in design reviews, troubleshooting integration issues, and providing technical documentation. Effective communication and teamwork are key, as you’ll be translating clinical needs into technical solutions and ensuring compliance with medical standards.

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

A Medical Device Embedded System Engineer typically needs a strong background in electrical or computer engineering, experience with embedded C/C++ programming, and a solid understanding of medical device regulations. Familiarity with microcontrollers, real-time operating systems (RTOS), and compliance standards like IEC 62304 is highly valuable, and certifications in embedded systems or medical device software can be advantageous. Strong problem-solving skills, attention to detail, and effective teamwork are essential soft skills for excelling in this position. These competencies ensure the development of safe, reliable, and regulatory-compliant medical devices that improve patient outcomes.

What is the difference between Medical Device Embedded System Engineer vs Medical Software Engineer?

AspectMedical Device Embedded System EngineerMedical Software Engineer
CredentialsBachelor's or higher in Electrical, Computer Engineering, or related; knowledge of embedded systemsBachelor's or higher in Computer Science, Software Engineering, or related; programming skills
Work EnvironmentDesigning and testing embedded hardware/software for medical devicesDeveloping medical software applications, often on PCs or servers
Industry UsageUsed in medical devices like pacemakers, imaging equipment, and monitorsUsed in healthcare software, EHR systems, and medical data analysis

The Medical Device Embedded System Engineer focuses on developing embedded hardware and firmware for medical devices, ensuring safety and compliance. In contrast, the Medical Software Engineer primarily develops software applications used in healthcare settings. Both roles require technical expertise but differ in their focus on hardware versus software development within the medical industry.

What job categories do people searching Medical Device Embedded System Engineer jobs in Rancho Cucamonga, CA look for? The top searched job categories for Medical Device Embedded System Engineer jobs in Rancho Cucamonga, CA are:
What cities near Rancho Cucamonga, CA are hiring for Medical Device Embedded System Engineer jobs? Cities near Rancho Cucamonga, CA with the most Medical Device Embedded System Engineer job openings:
Medical Device Embedded System Engineer jobs near you

Senior Quality Engineer I - Software

Staar Surgical

Monrovia, CA • On-site

$115K - $150K/yr

Full-time

Posted 14 days ago

Job description

MAIN JOB RESPONSIBILITIES / COMPETENCIES
1. Coordinate quality engineering activities supporting the Software as a Medical Device (SaMD), Quality System software, and Manufacturing software platforms to achieve business objectives.
2. Provide technical expertise through the software lifecycle, with a focus on SaMD, in the following areas: design control, risk analyses, verification/validation strategy, maintenance and change management.
3. Develop strategy as part of cross-functional teams to support the compliant and effective release of SaMD and other software applications.
4. Provide guidance and leadership on development / review of design control and validation policies and procedures, and resolutions to quality engineering issues. Act as an effective leader or team member in supporting quality disciplines, decisions, and practices.
5. Provide technical expertise to the risk documentation process.
6. Provide guidance and leadership on investigations involving software nonconformances, product or component failures, or customer complaints by leading or participating in the investigation process, technical troubleshooting, FMEA, hazard, or other risk analysis, determining root cause and recommending CAPA.
7. Participate in the preparation of nonconformance investigations and responses, and completion of corrective action plans as needed.
8. Provide guidance and leadership on design processes and site engineering functions to identify critical parameters and improve process quality.
9. Participate on Design Control New Product development teams; advise the team on design control requirements; develop, review and approve design control deliverables related to quality engineering and validations.
10. Other duties as assigned.
REQUIREMENTS
EDUCATION & TRAINING
• Bachelor's degree, preferably in Engineering or sciences.
• Advanced degree preferred.
• Certified Quality Engineer (CQE) or equivalent preferred
EXPERIENCE
• Five years' experience in validation and/or design control in the medical device software industry, including the practical application of FDA Quality System Regulation and ISO 13485; or equivalent combination of education/experience.
• Experience in medical device software change management required.
• Experience in vision care or intraocular lens industry preferred.
• General knowledge of medical device software requirements (IEC 62304, IEC 82304) required.
• Knowledge of international/ISO standards on ophthalmology preferred
• Applicant must be knowledgeable about regulatory/compliance/validation issues, be self-motivated, intelligent and reliable.
SKILLS
• Experience in writing technical documents, especially compliance and/or validation/quality assurance documents and protocols required.
• Proficiency in written and spoken English required.
• Excellent project management, organization, writing, communication and presentation skills required.
• Ability to communicate in a wide variety of communication styles and to influence and build consensus across cross-functional groups.
• Must have strong written and oral communication skills.
Pay range: $115K - $150K - Final compensation/salary will depend on experience.
STAAR Surgical is an Equal Employment Opportunity/Affirmative Action employer and all qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran or disability status, or any other characteristic protected by law.. #USA

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