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Home Based Medical Device Software Engineer Jobs in Washington

LKC Technologies is seeking an experienced Principal Software Engineer to serve as the technical ... Medical device development experience, including familiarity with design controls, risk management ...

Principal Software Engineer

Germantown, MD · On-site

$137K - $184K/yr

Medical device development experience, including familiarity with design controls, risk management ... The actual salary offered will be based on experience, skills, qualifications, market / business ...

Embedded Software Engineer (AFC Device)

Vienna, VA · On-site

$132K - $173K/yr

Embedded Software Engineer (AFC Device) About the Role STraffic America, headquartered in Vienna, Virginia, is a leading provider of Automatic Fare Collection (AFC) systems for major U.S. transit ...

Embedded Software Engineer (AFC Device)

Vienna, VA · On-site

$132K - $173K/yr

Embedded Software Engineer (AFC Device) About the Role STraffic America, headquartered in Vienna, Virginia, is a leading provider of Automatic Fare Collection (AFC) systems for major U.S. transit ...

Principal Software Engineer

Washington, DC

$152K - $205K/yr

Provide hands-on technical leadership for systems spanning IoT device control, smart home ... The package includes medical plans with company subsidies, a Health Savings Account (HSA) with a ...

Principal Software Engineer

Arlington, VA · On-site

$155K - $208K/yr

Provide hands-on technical leadership for systems spanning IoT device control, smart home ... The package includes medical plans with company subsidies, a Health Savings Account (HSA) with a ...

Principal Software Engineer

Tysons Corner, VA · On-site

$135K - $182K/yr

Provide hands-on technical leadership for systems spanning IoT device control, smart home ... The package includes medical plans with company subsidies, a Health Savings Account (HSA) with a ...

Principal Software Engineer

Mclean, VA

$136K - $183K/yr

Provide hands-on technical leadership for systems spanning IoT device control, smart home ... The package includes medical plans with company subsidies, a Health Savings Account (HSA) with a ...

Med - Software Engineer

Hanover, MD · On-site

$175K - $210K/yr

The software engineer will interface with and utilize device drivers from vendor provided SDK to implement custom business logic for the enterprise. The software engineer should have experience with ...

Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2026 or later with a Bachelor's degree in Computer Science, Software Engineering ...

Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2026 or later with a Bachelor's degree in Computer Science, Software Engineering ...

Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2026 or later with a Bachelor's degree in Computer Science, Software Engineering ...

Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2026 or later with a Bachelor's degree in Computer Science, Software Engineering ...

Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2026 or later with a Bachelor's degree in Computer Science, Software Engineering ...

Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2026 or later with a Bachelor's degree in Computer Science, Software Engineering ...

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Home Based Medical Device Software Engineer information

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

To excel as a Home Based Medical Device Software Engineer, you need strong programming skills (often in C/C++ or Python), a background in software engineering or computer science, and knowledge of medical device regulations such as IEC 62304. Familiarity with version control systems (like Git), embedded systems development tools, and experience with quality management systems are typically required, along with certifications in medical device software or related fields. Excellent problem-solving, attention to detail, and effective remote communication are standout soft skills for this role. These competencies are vital for developing safe, compliant, and reliable medical device software while collaborating efficiently from a remote environment.

What does a home based medical device software engineer do?

A Home Based Medical Device Software Engineer is responsible for designing, developing, testing, and maintaining software used in medical devices, all while working remotely. They ensure that the software complies with regulatory standards for safety and efficacy, often collaborating with cross-functional teams such as hardware engineers and regulatory specialists. Their work helps create software for devices like pacemakers, insulin pumps, or diagnostic equipment, ultimately improving patient care. Remote work enables flexibility, but also requires strong communication skills and a reliable home office setup.

What is the difference between Home Based Medical Device Software Engineer vs Medical Device Quality Assurance Specialist?

AspectHome Based Medical Device Software EngineerMedical Device Quality Assurance Specialist
CredentialsBachelor's in Software Engineering, Biomedical Engineering, or related field; certifications like CSTE or ISTQB beneficialBachelor's in Life Sciences, Quality Assurance, or related; certifications like CQE or ISO auditor preferred
Work EnvironmentRemote or home-based, collaborating with development teamsOn-site or remote, focusing on compliance and quality processes
Industry UsageDesigning and testing software for medical devicesEnsuring medical device manufacturing and software meet quality standards

While both roles support medical device development, the Home Based Medical Device Software Engineer focuses on software design and testing remotely, whereas the Medical Device Quality Assurance Specialist emphasizes compliance and quality assurance processes, often on-site or in regulated environments.

How does a home based medical device software engineer typically collaborate with cross-functional teams while working remotely?

As a Home Based Medical Device Software Engineer, collaboration with cross-functional teams is primarily achieved through virtual meetings, project management tools, and regular status updates. You’ll often work closely with QA specialists, regulatory affairs, hardware engineers, and clinical teams to ensure that the software meets safety and compliance standards. Effective communication and proactive engagement are essential, especially when troubleshooting issues or implementing new features. Most companies provide robust collaboration platforms and clear communication protocols to help remote engineers stay integrated with the broader team.

Medical Device & Technology Associate Attorney

Direct Counsel

Washington, DC

$235K - $310K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 13 days ago


Job description

Medical Device & Technology Associate Attorney

Direct Counsel is seeking a Medical Device & Technology Associate Attorney to join a prestigious Am Law firm in Washington, D.C.

This is an exceptional opportunity for an attorney interested in FDA regulatory law and medical device regulation to join a nationally recognized Food, Drug, Medical Device & Agriculture practice. The team advises medical device, biotechnology, pharmaceutical, and digital health companies on the full lifecycle of FDA regulatory compliance, including premarket submissions, post-market obligations, enforcement matters, and emerging issues involving artificial intelligence and software-based medical technologies.

Responsibilities
  • Advise clients on FDA regulatory requirements governing medical devices and related technologies.

  • Counsel clients on regulatory pathways for medical devices, including 510(k) notifications, Investigational Device Exemptions (IDEs), De Novo requests, and Premarket Approval Applications (PMAs).

  • Assist with FDA submissions, agency communications, and responses to deficiency letters and regulatory inquiries.

  • Advise on post-market compliance matters, including quality system regulations, recalls, adverse event reporting, and FDA enforcement issues.

  • Counsel clients on regulatory considerations affecting software as a medical device (SaMD), digital health technologies, artificial intelligence (AI), machine learning, cybersecurity, and diagnostic products.

  • Research and analyze evolving FDA regulations and related state, federal, and international regulatory developments.

  • Develop practical regulatory strategies that support innovative product development while managing compliance risks.

  • Collaborate with clients and multidisciplinary legal teams on sophisticated regulatory matters throughout the product lifecycle.

Qualifications
  • J.D. from an ABA-accredited law school.

  • Active membership in, or eligibility for admission to, the District of Columbia Bar.

  • Demonstrated interest in FDA regulatory law and medical device regulation.

  • Experience with FDA medical device matters is strongly preferred.

  • Experience at the FDA or within the medical device, pharmaceutical, or biotechnology industries is a plus.

  • Scientific, engineering, health sciences, or biotechnology background is preferred but not required.

  • Excellent legal research, analytical, drafting, and communication skills.

  • Strong academic credentials and the ability to thrive in a collaborative, fast-paced, client-focused environment.

Compensation & Benefits
  • Salary: $235,000-$310,000, commensurate with experience and qualifications.

  • Comprehensive benefits package, including:

    • Medical, dental, and vision insurance

    • 401(k) retirement plan

    • Paid time off

    • Annual performance and discretionary bonus eligibility

    • Relocation assistance, where applicable