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Home Based Medical Device Software Engineer Jobs

Diality

Director, Software Engineering

Irvine, CA · Hybrid

$223K - $260K/yr

... Linux-based systems, BSP, bare-metal hardware/software integration, software debugging, and ... engineer contractors. * Familiarity with cloud-connected medical device systems, mobile ...

Diality Inc

Director, Software Engineering

Irvine, CA · On-site

$223K - $260K/yr

... Linux-based systems, BSP, bare-metal hardware/software integration, software debugging, and ... engineer contractors. * Familiarity with cloud-connected medical device systems, mobile ...

Teleflex

Sr. Engineer, Software Dev, R&D

Morrisville, NC · On-site

$114K - $151K/yr

... the home of Arrow, Barrigel, Deknatel, LMA, Pilling, QuikClot, Rusch, UroLift and Weck - trusted ... Design and develop medical device software that is high quality, safe, secure and compliant. Lead ...

Alcon

Principal, Software Engineer

Lake Forest, CA · On-site

$143K - $192K/yr

The Principal Software Engineer, Medical Device Systems is responsible for maintaining, enhancing ... FPGA-based systems, LabVIEW, and RTOS environments . The engineer will investigate software ...

Rangam Consultants

Software Engineer

San Diego, CA · On-site

Support compliance considerations related to regulated medical device software development practices. * Document findings and recommendations to facilitate efficient handoff to permanent engineering ...

Neuralink

Software Design Quality Engineer

Austin, TX · On-site

The Software Design Controls Engineer will own software design control strategy, processes ... Own software design control impact assessments for design changes within the medical device design ...

Spruce Infotech

Software Engineer C++

Arden Hills, MN · On-site

... medical device systems. Work with a team of highly skilled engineers to deliver groundbreaking ... Develop software for testing platforms and complex software tools. * Integrate software designs ...

Abbott

Sr. Embedded Software Engineer

New Brighton, MN

$131K - $171K/yr

Provide technical support for all phases of the medical device software lifecycle, including ... C programming for embedded systems, including ARM based microcontrollers. * Systems engineering ...

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Home Based Medical Device Software Engineer information

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$63.5K

$147.5K

$205.5K

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

As of Aug 25, 2026, the average yearly pay for home based medical device software engineer in the United States is $147,524.00, according to ZipRecruiter salary data. Most workers in this role earn between $120,000.00 and $173,000.00 per year, depending on experience, location, and employer.

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 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.

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.

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.

What cities are hiring for Home Based Medical Device Software Engineer jobs?

Cities with the most Home Based Medical Device Software Engineer job openings:

What are the most commonly searched types of Medical Device Software Engineer jobs?

The most popular types of Medical Device Software Engineer jobs are:

What states have the most Home Based Medical Device Software Engineer jobs?

States with the most job openings for Home Based Medical Device Software Engineer jobs include:

Home Based Medical Device Software Engineer jobs near you

Software Design Control Engineer

Jobtailor

San Francisco, CA • On-site

$130 - $190/hr

Other

Posted 6 days ago

Job description

  • Work alongside software engineers to author, review, and maintain comprehensive design control documentation, including Software Requirements Specifications, Architecture & Design Documents, and Traceability Matrices.
  • Ensure software development processes align with IEC 62304 (Medical Device Software Lifecycle), ISO 13485, and FDA 21 CFR Part 820 regulations.
  • Author and maintain software risk management files, including Software FMEAs per ISO 14971.
  • Produce software verification and validation (V&V) protocols and reports in coordination with the engineering and test teams to ensure full traceability.
  • Compile and organize necessary software technical documentation for regulatory submissions.
  • Maintain and update software documentation for post-market surveillance, CAPAs, and software updates.
Requirements
  • 5+ years of experience in the medical device industry, specifically working with software‑driven or connected medical devices (Class II or Class III).
  • A Bachelor’s degree in Computer Science, Biomedical Engineering, Software Engineering, or a related field, or equivalent practical engineering experience.
  • Demonstrated experience writing, reviewing, and managing formal medical device software documentation (Design History Files, Traceability Matrices).
  • Proven track record of taking a medical device software product through a successful FDA clearance/approval process and subsequent launch.
  • Deep familiarity with IEC 62304, ISO 14971, and FDA Software Validation Guidelines.
  • Experience with modern software development workflows (e.g. Git, Jira) and quality system tools (e.g. Greenlight Guru, Arena, Matrix Requirements, or Jama).
Core Competencies

Expertise in authoring and managing medical device software documentation, including compliance with IEC 62304, ISO 14971, and FDA regulations. Proven ability to navigate the FDA clearance process for software‑driven medical devices.

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