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Medical Device Embedded Software Engineer Jobs in Carteret, NJ

... embedded software that power Clarapath's advanced SectionStar™ and TrimStar Pro™ platforms ... medical device and robotics technologies that improve laboratory workflows and patient outcomes.

Creative and innovative engineers with prior embedded software engineering experience who can design and develop innovative security solutions on the most complex processors. BAE Systems is currently ...

Entry level Embedded Engineer

New York, NY · On-site

$143K - $189K/yr

C/C++/Python Embedded Software Engineer with Linux & hardware interface experience - #1 Importance: Write complete code.... - Design software features to meet product requirements - Write technical ...

Entry level Embedded Engineer

New York, NY · On-site

$143K - $189K/yr

C/C++/Python Embedded Software Engineer with Linux & hardware interface experience - #1 Importance: Write complete code.... - Design software features to meet product requirements - Write technical ...

Showing results 21-40

Medical Device Embedded Software Engineer information

See Carteret, NJ salary details

$71K

$155.6K

$176.5K

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

As of Aug 24, 2026, the average yearly pay for medical device embedded software engineer in Carteret, NJ is $155,605.00, according to ZipRecruiter salary data. Most workers in this role earn between $133,400.00 and $175,500.00 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 Carteret, NJ?

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

What cities near Carteret, NJ are hiring for Medical Device Embedded Software Engineer jobs?

Cities near Carteret, NJ with the most Medical Device Embedded Software Engineer job openings:

Software Controls Engineer

Clarapath Inc.

Manhattan, NY • On-site

$110 - $170/hr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 5 days ago


Job description

Clarapath is a medical robotics company based in Westchester County, NY, dedicated to transforming and modernizing laboratory workflows. Our mission is to improve patient care by increasing efficiency, reducing costs, and enhancing the quality and consistency of laboratory processes.

Our portfolio includes SectionStar™ and TrimStar Pro™, innovative electro‑mechanical systems designed to automate and elevate critical steps in the histology workflow. SectionStar™ delivers high‑quality, consistent tissue sections, while TrimStar Pro™ streamlines and standardizes the trimming process - together enabling laboratories to operate with greater precision, throughput, and reliability.

At Clarapath, we bring together experts across engineering, data science, robotics, healthcare innovation, and laboratory operations. Our R&D team drives innovation, product enhancements, and a strong pipeline of new solutions, while our manufacturing team oversees production and quality control at our ISO‑certified facility. Also based in our New York headquarters are our sales, marketing, administrative, and service teams, who work closely together to ensure every customer receives a seamless, personalized experience at every touchpoint.

Role Summary:

The Software Controls Engineer will play a key role in the design, development, implementation, and continuous improvement of the control systems and embedded software that power Clarapath's advanced SectionStar™ and TrimStar Pro™ platforms. This individual will contribute to all phases of the product development lifecycle, from system architecture and algorithm development through implementation, testing, verification, manufacturing support, and field deployment. Working closely with mechanical, electrical, software, manufacturing, quality, and customer‑facing teams, the Software Controls Engineer will develop reliable, scalable, and maintainable control software that meets performance, safety, and regulatory requirements. We are seeking a hands‑on engineer who enjoys solving complex automation and motion control challenges, thrives in a collaborative and fast‑paced environment, and is passionate about developing innovative medical device and robotics technologies that improve laboratory workflows and patient outcomes.

  • Design, develop, implement, and maintain embedded software and control algorithms for motion control systems, actuators, sensors, and peripheral devices
  • Develop software architecture and control logic using C/C++, Python, and other appropriate programming languages
  • Design and optimize closed‑loop control systems for precision motion applications utilizing servo motors, stepper motors, encoders, and other electromechanical components
  • Collaborate with Electrical and Mechanical Engineering teams to integrate hardware and software into complete system solutions.
  • Develop communication interfaces using protocols such as CAN, RS‑232, RS‑485, Ethernet, USB, SPI, I2C, and UART.
  • Create software requirements, design specifications, verification protocols, and technical documentation in compliance with medical device design controls
  • Participate in system architecture discussions and technical design reviews
  • Perform software debugging, root cause analysis, and issue resolution throughout development and post‑release support
  • Develop automated testing tools and software validation procedures to improve product quality and reliability
  • Support prototype development, system integration, and engineering verification testing
  • Assist Manufacturing and Service teams with software releases, troubleshooting, and continuous product improvements.
  • Participate in risk management activities including software hazard analysis, FMEA, and mitigation implementation
  • Support regulatory submissions and compliance efforts by generating appropriate documentation and maintaining design history files.
  • Contribute to continuous improvement initiatives focused on software quality, maintainability, cybersecurity, and system performance.
  • Provide technical support during customer installations, field investigations, and product issue resolution as needed
Qualifications:
  • Bachelor’s degree in Computer Engineering, Electrical Engineering, Computer Science, Software Engineering, or a related engineering discipline
  • 3–7 years of experience developing embedded software or control systems for electromechanical products
  • Strong programming experience in C/C++
  • Experience with embedded Linux or real‑time operating systems (RTOS)
  • Experience developing motion control software for precision electromechanical systems
  • Strong understanding of software architecture, object‑oriented programming, and software design principles
  • Experience interfacing with sensors, motors, actuators, and industrial communication protocols
  • Familiarity with source control systems such as Git
  • Experience using debugging tools including oscilloscopes, logic analyzers, and protocol analyzers.
  • Strong analytical, troubleshooting, and problem‑solving skills
  • Excellent written and verbal communication skills
  • Ability to work effectively in a collaborative, multidisciplinary engineering environment
  • Experience developing software for medical devices or other regulated industries, a plus
  • Knowledge of IEC 62304 software lifecycle processes, a plus
  • Familiarity with ISO 13485 quality management systems, a plus
  • Experience with FDA Design Controls and Design History Files (DHF), a plus
  • Experience developing software for robotics, automation, or precision instrumentation, a plus
  • Knowledge of machine vision integration, image processing, or computer vision, a plus
  • Experience with Python scripting for automation and test development, a plus
  • Familiarity with cybersecurity best practices for connected medical devices, a plus
  • Experience with Agile software development methodologies, a plus
  • Knowledge of Jira, Confluence, and requirements management tools, a plus
  • Experience with hardware‑in‑the‑loop (HIL) testing or simulation environments, a plus
Company Offers:
  • Competitive salary, commensurate with experience and education
  • Comprehensive benefits package available: (healthcare, vision, dental and life insurances; 401k; PTO and holidays)
  • A collaborative and diverse work environment where our teams thrive on solving complex challenges
  • Ability to file IP with the company
  • Connections with world class researchers and their laboratories
  • Collaboration with strategic leaders in healthcare and pharmaceutical world
  • A mission driven organization where every team member will be responsible for changing the standards of delivering healthcare

Clarapath is proud to be an equal opportunity employer. We are committed to providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status. In addition to federal law requirements, Clarapath complies with applicable state and local laws governing nondiscrimination in employment. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, rebates, leaves of absence, compensation, and training.

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