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Medical Device Embedded System Engineer Jobs in Secaucus, NJ

Getinge

Engineer II, R&D Systems - Wayne, NJ

Wayne, NJ · On-site

$100 - $105/hr

Strong understanding of medical device development methodologies and regulatory requirements ... execution of system-level testing of medical devices * Hands‑on ability to work safely and ...

New

Crane Company

Firmware Engineer

Saddle Brook, NJ · On-site

This role requires a technical expertise in embedded systems, firmware development, hardware ... Implement device drivers, communication protocols, bootloaders, and real-time control algorithms.

Crane Company

Firmware Engineer

Saddle Brook, NJ

This role requires a technical expertise in embedded systems, firmware development, hardware ... Implement device drivers, communication protocols, bootloaders, and real-time control algorithms.

Crane Co.

Firmware Engineer

Saddle Brook, NJ · On-site

$95 - $120/hr

Firmware & Embedded Systems Development*** Design, develop, test, and maintain embedded firmware ... Implement device drivers, communication protocols, bootloaders, and real-time control algorithms.

AITAN

Systems Engineer, Robotics Integration

New York, NY · On-site +1

$180K - $220K/yr

Develop integration scripts, test harnesses, and automated validation tools to verify system ... Hands-on embedded software experience: C/C++ firmware, RTOS concepts, device drivers, and board ...

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All JobsMedical Device Embedded System Engineer JobsMedical Device Embedded System Engineer Jobs in Secaucus, NJ

Medical Device Embedded System Engineer information

See Secaucus, NJ salary details

$63.5K

$139.6K

$195.2K

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

As of Sep 6, 2026, the average yearly pay for medical device embedded system engineer in Secaucus, NJ is $139,564.00, according to ZipRecruiter salary data. Most workers in this role earn between $113,400.00 and $166,200.00 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 are popular job titles related to Medical Device Embedded System Engineer jobs in Secaucus, NJ?

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

What job categories do people searching Medical Device Embedded System Engineer jobs in Secaucus, NJ look for?

The top searched job categories for Medical Device Embedded System Engineer jobs in Secaucus, NJ are:

What cities near Secaucus, NJ are hiring for Medical Device Embedded System Engineer jobs?

Cities near Secaucus, NJ with the most Medical Device Embedded System Engineer job openings:

Medical Device Embedded System Engineer jobs near you
Infographic showing various Medical Device Embedded System Engineer job openings in Secaucus, NJ as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 16% Part Time, 1% Temporary, and 6% Contract. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $139,564 per year, or $67.1 per hour.

Engineer II, R&D Systems - Wayne, NJ

Getinge

Wayne, NJ • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 5 days ago

Getinge rating

9.3

Company rating: 9.3 out of 10

Based on 14 frontline employees who took The Breakroom Quiz

13th of 499 rated machine equipment manufacturers

Job description

With a passion for life
Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. To make a true difference for our customers - and to save more lives, we need team players, forward thinkers, and game changers.
Are you looking for an inspiring career? You just found it.
Job Overview
The Systems Engineer will be responsible for providing technical input to a team of systems and cross-functional engineers. You will support the development, improvement, verification, and troubleshooting of on-market electromechanical medical devices, including hands-on work in the engineering lab to support testing, data collection, and root cause assessment. A key aspect of this role involves the use of tools such as Excel and JAMA for requirements management and traceability, ensuring that all project deliverables meet the specified criteria. The ideal candidate will support implementation of changes and is capable of working with a degree of flexibility while maintaining the current product and driving improvements in our systems engineering practices. The systems engineer will ensure that development, remediation, and investigation activities are compliant with internal development processes and regulatory requirements specifically 21 CFR 820.30.
Job Responsibilities and Essential Duties
  • Support the development and improvement of on-market electromechanical medical devices, ensuring that solutions are scalable, maintainable, and meet regulatory requirements.
  • Utilize tools such as Excel and JAMA to manage requirements, track progress, and ensure traceability throughout the project.
  • Work in the engineering lab to support system-level testing, troubleshooting, data collection, test setup execution, and root cause assessment for product issues, complaints, CAPAs, and design changes.
  • Collaborate with cross-functional teams to define project scope, objectives, and deliverables.
  • Participate in design reviews and provide constructive feedback to team members to ensure high-quality designs.
  • Maintain the current product while implementing innovative solutions and improvements.
  • Support the development and remediation of electromechanical medical devices, ensuring that solutions are scalable, maintainable, and meet regulatory requirements.
  • Collaborate with cross-functional teams to define project scope, objectives, and deliverables.
  • Participate in design reviews and provide constructive feedback to team members to ensure high-quality designs.
  • Maintain the current product while implementing innovative solutions and improvements.
  • Drive product improvements based on data and feedback.
  • Ensure compliance with all relevant regulatory requirements and standards.

Minimum Requirements
  • BS in Systems, Biomedical, Electrical, Software, or related Engineering discipline with 4+ years of related systems engineering, design controls, medical device, product development, engineering lab testing, or root cause investigation experience
  • MS or PhD in Systems, Biomedical, Electrical, Software, or related Engineering discipline with 2+ years of related systems engineering, design controls, medical device, product development, engineering lab testing, or root cause investigation experience

Required Knowledge, Skills, and Abilities
  • Experience consistent with an Engineer II role on this team, including demonstrated ability to work with moderate independence in regulated product development, system-level testing, troubleshooting, objective evidence collection, and root cause assessment.
  • Strong track record of supporting the development of electromechanical medical devices.
  • Proficiency in using tools such as JAMA for requirements management and traceability.
  • Strong understanding of medical device development methodologies and regulatory requirements.
  • Excellent problem-solving skills and the ability to think critically and strategically.
  • Strong communication and interpersonal skills, with the ability to effectively collaborate with team members and stakeholders.
  • Participate in technical meetings with cross-functional team members.
  • Knowledge of requirements development, traceability, and allocation
  • Knowledge of medical device risk management, including ISO 14971:2012; Knowledge of ISO 13485:2016.
  • Knowledge of design verification and validation concepts, including the planning and execution of system-level testing of medical devices
  • Hands-on ability to work safely and effectively in an engineering lab environment to execute test setups, collect objective evidence, support troubleshooting, and contribute to root cause investigations.
  • Medical Device experience including thorough understanding of Design Controls (21 CFR 820.30).
  • Working knowledge of FDA and International Standards requirements as related to capital equipment.
  • Experience with Requirements Management Tools (such as JAMA)
  • Strong organizational and technical writing skills
  • Excellent written and verbal communication skills
  • Demonstrates a learning mindset, curiosity, and willingness to ask questions, seek feedback, and apply coaching from senior engineers and cross-functional partners.
  • Uses clear communication to share observations, document test results, raise concerns, and align with team members on assigned work.
  • Works collaboratively in a team environment, demonstrating reliability, accountability for assigned tasks, and openness to different technical perspectives.
  • Maintains attention to detail and follow-through when collecting data, documenting objective evidence, tracking action items, and escalating issues appropriately.

Salary range: $100-105K; Target bonus 8%
About us
With a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The offering includes products and solutions for intensive care, cardiovascular procedures, operating rooms, sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the products are sold in more than 135 countries.
Benefits at Getinge:
At Getinge, we offer a comprehensive benefits package, which includes:
  • Health, Dental, and Vision insurance benefits
  • 401k plan with company match
  • Paid Time Off
  • Wellness initiative & Health Assistance Resources
  • Life Insurance
  • Short and Long Term Disability Benefits
  • Health and Dependent Care Flexible Spending Accounts
  • Commuter Benefits
  • Parental and Caregiver Leave
  • Tuition Reimbursement

Getinge is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, pregnancy, genetic information, national origin, disability, protected veteran status or any other characteristic protected by law. Reasonable accommodations are available upon request for candidates taking part in all aspects of the selection process.

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About Getinge

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Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Dr Wayne, NJ, US

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