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Medical Device Embedded Software Engineer Jobs in Tracy, CA

Abbott

Systems Engineer

Pleasanton, CA · On-site

$75 - $80/hr

Coordinate end-to-end integration activities across embedded firmware, mechanical components ... Medical device experience, particularly with connected or software-enabled medical devices.

Elroy Air

Senior Software Engineer, Operator Tools

Byron, CA · On-site +1

$135K - $178K/yr

Communication interfaces between desktop tools and embedded systems (serial, UDP, custom protocols ... Comprehensive medical benefits * 401(k) with company contribution + Roth IRA * Free daily lunch ...

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All JobsMedical Device Embedded Software Engineer JobsMedical Device Embedded Software Engineer Jobs in Tracy, CA

Medical Device Embedded Software Engineer information

See Tracy, CA salary details

$75.4K

$165.1K

$187.3K

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

As of Aug 23, 2026, the average yearly pay for medical device embedded software engineer in Tracy, CA is $165,115.00, according to ZipRecruiter salary data. Most workers in this role earn between $141,600.00 and $186,200.00 per year, depending on experience, location, and employer.

What is a medical device embedded software engineer?

Medical Device Embedded Software Engineers are professionals who design, develop, and maintain the specialized software that runs on hardware inside medical devices, such as pacemakers, infusion pumps, and imaging machines. They ensure that the software meets strict regulatory standards for safety, reliability, and performance. Their work involves programming, testing, debugging, and documenting embedded code, as well as collaborating with hardware engineers and regulatory teams to bring safe and effective medical products to market.

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

To thrive as a Medical Device Embedded Software Engineer, you need a strong background in embedded systems design, C/C++ programming, and a degree in electrical engineering, computer engineering, or a related field. Familiarity with real-time operating systems (RTOS), hardware-software integration, and industry standards like IEC 62304 or FDA regulations is typically required. Attention to detail, strong problem-solving abilities, and effective teamwork are vital soft skills for this role. These competencies are crucial for developing reliable, safe, and compliant software that meets stringent healthcare requirements.

What are some common challenges faced by medical device embedded software engineers when working on cross-functional teams?

Medical Device Embedded Software Engineers often collaborate closely with hardware engineers, regulatory specialists, and quality assurance teams. A common challenge is ensuring that software requirements align with hardware limitations and regulatory standards, which can necessitate frequent adjustments and clear documentation. Additionally, balancing the pace of software development with the rigorous testing and validation processes required for medical devices can be demanding. Effective communication and adaptability are essential to navigate these multidisciplinary interactions and deliver safe, compliant products.

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

AspectMedical Device Embedded Software EngineerFirmware Engineer
CredentialsBachelor's in Electrical, Computer Engineering, or related; often certifications in medical device standardsBachelor's in Electrical, Computer Engineering, or related; certifications vary by industry
Work EnvironmentMedical device companies, regulated environments, quality assurance focusConsumer electronics, industrial, or embedded systems companies
Industry UsagePrimarily in healthcare, medical device manufacturingBroader tech sectors, including consumer electronics and industrial systems
Search & Comparison IntentHigh overlap in embedded systems, safety standards, and certification requirements

The Medical Device Embedded Software Engineer and Firmware Engineer roles share core skills in embedded systems development. However, the Medical Device Embedded Software Engineer focuses specifically on medical device safety, regulatory compliance, and working within healthcare environments. Firmware Engineers may work across various industries without the strict medical standards, making the Medical Device Embedded Software Engineer role more specialized in healthcare applications.

What are popular job titles related to Medical Device Embedded Software Engineer jobs in Tracy, CA?

For Medical Device Embedded Software Engineer jobs in Tracy, CA, the most frequently searched job titles are:

What job categories do people searching Medical Device Embedded Software Engineer jobs in Tracy, CA look for?

The top searched job categories for Medical Device Embedded Software Engineer jobs in Tracy, CA are:

What cities near Tracy, CA are hiring for Medical Device Embedded Software Engineer jobs?

Cities near Tracy, CA with the most Medical Device Embedded Software Engineer job openings:

Medical Device Embedded Software Engineer jobs near you
Infographic showing various Medical Device Embedded Software Engineer job openings in Tracy, CA 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 $165,115 per year, or $79.4 per hour.

Principal Hardware Engineer - Fluidics - Pleasanton, CA

Calyxo

Pleasanton, CA • On-site

Full-time

Medical, Retirement, PTO

Re-posted 14 days ago

Job description

Calyxo, Inc. is a medical device company headquartered in Pleasanton, California, USA. The company was founded in 2016 to address the profound need for improved kidney stone treatment. Kidney stone disease is a common, painful condition that consumes vast amounts of healthcare resources each year. Our team is led by executives and investors with a proven track record of commercializing paradigm-shifting devices to meet unmet needs within urology.
Are you ready to change the future of kidney stone treatment? We are seeking high achievers who want to be part of a dynamic team working in a fun, diverse atmosphere.
Summary:
We are seeking a highly skilled and innovative hardware engineer to lead development of advanced fluidic subsystems in kidney stone treatment. This role focuses on the design and control of irrigation and aspiration systems, combining pumps, valves, sensors, tubing sets, and embedded software into safe and reliable products. This is a hands-on technical leadership role for an engineer who enjoys developing both hardware and control algorithms, working across mechanical, electrical, and software boundaries to deliver clinically robust performance. This role requires ensuring that all engineering efforts comply with industry standards and regulatory requirements, while aligning with strategic business objectives.
In This Role, You Will:
  • Own and architect end-to-end fluid control systems across capital equipment and disposable instruments/tubing sets.
  • Define and drive development of control algorithms to regulate irrigation and aspiration under varying clinical and patient conditions.
  • Define system/sub-system performance requirements for flow, pressure, responsiveness, alarms, and fault detection.
  • Perform system modeling, trade studies, prototyping and bench testing to educate key component selection (pumps, sensors, actuators), validate decisions and de-risk technical challenges.
  • Individually contribute to mechanical/electromechanical design for critical fluidics subsystem components and assemblies and provide expert design review of other team-members designs.
  • Lead cross-functional alignment across internal teams and external partners to ensure architectural integrity, V&V readiness, and production scalability.
  • Collaborate with Systems & Test Engineering to drive design verification test planning and execution for fluid control hardware subsystems.
  • Lead hardware sub-system risk management activities (e.g., FMEA).
  • Organize system/sub-system-level technical design reviews to ensure coherent design across hardware, firmware and software interfaces.
  • Collaborate with suppliers and internal operations representatives to perform root cause investigation, component lifecycle management and continuous improvement.
  • Provide deep subject matter expertise toward the technology roadmap for fluidics and controls and related research endeavors.
  • Partner closely with mechanical, electrical, software, systems, clinical, quality, regulatory and other cross-functional teams to bring prototypes to the market.
  • Mentor junior and non-specialist engineering talent, promoting a collaborative and high-performance work environment.

Who You Will Report To:
  • Director, Vision and Sensor Systems

Requirements:
  • Bachelor's degree in Mechanical Engineering, Biomedical Engineering, Electrical Engineering, Mechatronics, or a related discipline. Master's or PhD in a relevant engineering discipline preferred.
  • 15+ years of experience developing fluidic, mechatronic, or control systems in a regulated product environment.
  • Experience with owning end-to-end hardware system architectures for fluidic control systems. Preferred familiarity with disposable fluidic component design and reusable/disposable system interfaces.
  • Proven experience developing and tuning closed-loop control systems for electromechanical hardware. Preferred experience with irrigation and aspiration systems, endoscopic or urological devices, or surgical fluid management platforms. Experience with pressure, flow, air-in-line, or occlusion detection preferred.
  • Experience prototyping and testing systems at the bench and subsystem level, including proficiency with prototype embedded software development (e.g., C/C++, Python, or similar) to support hardware designs.
  • Strong first-principles thinker with expert-level fundamentals in fluid dynamics applied to precision fluid delivery in complex devices.
  • Ability to design experiments, analyze data, and translate results into design improvements.
  • Clear technical communication skills and ability to influence across multidisciplinary teams.
  • Experience leading external vendors and contract development firms.
  • Exceptional structured problem-solving skills and experience leading multifunctional technical project teams through all development lifecycle phases.
  • Prior work on medical devices or other safety-critical products, including knowledge of IEC 60601, ISO 13485, and medical device design controls.
  • Experience in requirements definition, design reviews, design verification, change management and risk control
  • Ability to travel domestically and internationally up to 10% of the time.

What We Offer:
At Calyxo, you will be part of a knowledgeable, high-achieving, experienced, and fun team. You will work in a diverse work environment with experienced, proven leaders and have an opportunity to shape our company culture. You will experience constant learning and dynamic challenges to help you grow and be the best version of yourself.
We also offer an attractive compensation package, which includes:
  • A competitive base salary of $250,000 - $270,000 and variable incentive plan
  • Stock options - ownership and a stake in growing a mission-driven company
  • Employee benefits package that includes 401(k), healthcare insurance and paid vacation

Calyxo is deeply committed to fostering an environment where diversity and inclusion are not only valued but also prioritized. We believe a diverse and inclusive community empowers us to act courageously, care deeply, and dream boldly to impact people in big ways. Diverse viewpoints bring diverse capabilities, which strengthen our focus and fuel our growth.
Calyxo is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status or any other applicable legally protected characteristics
Legal authorization to work in the United States is required. In compliance with federal law, all persons hired will be required to verify their identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire.
Disclaimer:
At Calyxo, we prioritize a transparent and structured interview process to ensure the best fit for both our candidates and our team. Please be aware of the following:
  • Structured Interview Process: Our hiring process includes multiple stages of interviews where you will have the opportunity to communicate directly with Calyxo employees. This ensures that you gain a comprehensive understanding of the role and our company culture.
  • Verification of Identity: We do not extend job offers without first meeting candidates, either virtually or in person. This step is crucial to maintain the integrity of our hiring process and to ensure mutual alignment.
  • Beware of Scams: Calyxo will never request sensitive personal information, such as your full name, address, phone number, or identification documents, via email or online forms before an official interview. Calyxo representatives will always contact you using an email format of firstname.lastname@calyxoinc.com. If you receive a request for information from any other domain, please contact us directly at info@calyxoinc.comto verify the legitimacy of the communication.

We appreciate your interest in joining Calyxo and look forward to getting to know you through our official channels.

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