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Medical Device Embedded Software Engineer Jobs in Delaware

Cisco

Software Engineer, Backend

Dover, DE · On-site

$152K - $219K/yr

... the software development lifecycle. Preferred Qualifications * Programming experience in Rust ... S. employees are offered benefits, subject to Cisco's plan eligibility rules, which include medical ...

Genesis10

Senior Software Engineer - Hybrid

Wilmington, DE · On-site

$66.41 - $74.41/hr

Genesis10 is currently seeking a Senior Software Engineer - Hybrid position with a Global Financial ... Medical, Dental, Vision * Health Savings Account * Voluntary Hospital Indemnity (Critical Illness ...

Hologic

Lead Cloud DevOps Platform Engineer

Newark, DE · On-site

$51.50 - $70.75/hr

... medical device software. As the primary bridge between cloud strategy and day-to-day developer operations, you will design, build, and maintain our Internal Developer Platform (IDP), ensuring our ...

Hologic Inc.

Lead Cloud DevOps Platform Engineer

Newark, DE · Remote

$51.50 - $70.75/hr

... medical device software. As the primary bridge between cloud strategy and day-to-day developer operations, you will design, build, and maintain our Internal Developer Platform (IDP), ensuring our ...

Hologic

Manufacturing Quality Engineer

Newark, DE · On-site

$72K - $93K/yr

Provide quality engineering support to Operations, Engineering and R&D in the design and ... Working knowledge of medical device Quality System Regulations (21CFR820), ISO 13485 and MDD ...

Hologic Inc.

Manufacturing Quality Engineer

Newark, DE · On-site

$72K - $93K/yr

Provide quality engineering support to Operations, Engineering and R&D in the design and ... Working knowledge of medical device Quality System Regulations (21CFR820), ISO 13485 and MDD ...

HK Recruiting

SR Electrical Engineer, R&D, NPD

Newark, DE · On-site

$105K - $136K/yr

Experience in an FDA regulated medical device industry is beneficial. Skills * Advanced knowledge ... Ability to write embedded code to test designs is beneficial. Must follow all applicable FDA ...

Hologic Inc.

Lead Software Engineer, Full Stack

Newark, DE · On-site +1

$128K - $200K/yr

As Lead Software Engineer, you'll drive the design, development, and improvement of tools ... NET to create user-facing applications for our medical devices, and play a key role in technical ...

Agilent

R&D Engineer

Wilmington, DE · On-site

$116K - $182K/yr

... software engineers, to create a complete system. As part of those projects, you will also work with ... an embedded processor to transport sample vials to an automated liquid sampling device.

Agilent

R&D Engineer

Wilmington, DE · On-site

$116K - $182K/yr

... software engineers, to create a complete system. As part of those projects, you will also work with ... an embedded processor to transport sample vials to an automated liquid sampling device.

Fusion Life Sciences

System Engineers

Newark, DE · On-site

System Engineer Location: Newark, DE Long Term Contract Job Overview: We are seeking highly skilled ... The ideal candidate will have 5-8 years of experience in the medical device industry, with a strong ...

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Medical Device Embedded Software Engineer information

See Delaware salary details

$70.1K

$153.5K

$174.2K

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

As of Jul 14, 2026, the average yearly pay for medical device embedded software engineer in Delaware is $153,516.00, according to ZipRecruiter salary data. Most workers in this role earn between $131,600.00 and $173,100.00 per year, depending on experience, location, and employer.

What are Medical Device Embedded Software Engineers?

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 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 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 are popular job titles related to Medical Device Embedded Software Engineer jobs in Delaware? For Medical Device Embedded Software Engineer jobs in Delaware, the most frequently searched job titles are:
What job categories do people searching Medical Device Embedded Software Engineer jobs in Delaware look for? The top searched job categories for Medical Device Embedded Software Engineer jobs in Delaware are:
What cities in Delaware are hiring for Medical Device Embedded Software Engineer jobs? Cities in Delaware with the most Medical Device Embedded Software Engineer job openings:
Medical Device Embedded Software Engineer jobs near you

Lead Compliance Engineer, R&D

HK Recruiting

Newark, DE

Other

Posted 13 days ago

Job description

Our client is a global leader in medical device innovation, dedicated to improving lives through advanced technology and rigorous quality standards. As we expand our portfolio and reach, we are looking for a talented Lead Compliance Engineer to join our Research & Development (R&D) team and drive product compliance for our global markets.

As the Lead Compliance Engineer, R&D, you will define and execute product compliance strategies, policies, and processes to ensure medical products meet regulatory standards and achieve necessary certifications (e.g., ISO, FCC, UL, IEEE). Serving as the technical subject matter expert, you will work closely with regulatory agencies, participate in product design reviews, and guide cross-functional teams to prevent compliance issues from initial design through production and delivery.

You will oversee both internal and external compliance testing, maintain documentation, and ensure supplier adherence to domestic and international requirements. With your wide-ranging experience, you’ll resolve complex issues, determine new methods and procedures, and may coordinate activities of other personnel as a team lead.

Key Responsibilities:

  • Develop and implement compliance strategies for global regulatory standards (EU MDR, EMC/EMI, safety compliance, etc.) throughout the product lifecycle.
  • Serve as the primary technical expert for regulatory compliance, supporting Program Management, Regulatory Assurance, and R&D teams.
  • Participate in product design reviews, identify applicable regulatory standards, and provide training to prevent compliance issues.
  • Oversee EMC, environmental, and IEC 60601-1 compliance testing at certified labs; act as liaison with agencies such as UL, CSA, TUV, BSI.
  • Drive compliance activities for new product launches, post-launch changes, and corrective actions to ensure ongoing regulatory compliance.
  • Support internal and third-party audits, prepare and review documentation for test labs and regulatory bodies.
  • Create compliance program plans, certification test plans, verification procedures, and reports.
  • Collaborate with engineering, marketing, systems, and manufacturing teams to implement compliance requirements into product definitions.
  • Manage multiple projects and priorities, contributing to CAPA, cost reduction, EOL, and operations support projects.
  • Mentor and train junior engineers as needed.

What we are looking for:

  • Bachelor’s degree required; Master’s or PhD in a technical field strongly preferred.
  • 8+ years of experience (or 6+ years with Master’s, 3+ years with PhD) in compliance testing for product devices and international certifications.
  • Experience with wireless technologies (Wi-Fi, RFID) and electrical test equipment (spectrum analyzers, vector network analyzers, signal generators).
  • Strong understanding of medical device compliance and safety standards, device manufacturing, and product lifecycle processes.
  • Proficient in EMC design concepts, lab test equipment (multi-meters, oscilloscopes, spectrum analyzers, etc.).
  • Ability to troubleshoot and resolve complex EMC issues.
  • Experience leading cross-functional teams and projects.
  • Logical thinking, mature engineering judgement, and strong analytical/problem-solving skills.
  • Effective collaboration and communication skills with technical and non-technical colleagues.
  • Proficiency in revision control and at least one software language (e.g., Python).
  • Familiarity with FDA, FAA, DoD, ISO environments and risk assessment management.
  • Proficient in Microsoft Office Suite (Excel, Word, PowerPoint).
  • Ability to mentor and train junior engineers is a plus.

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