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Home Based Medical Device Software Engineer Jobs

Bayer Inc.

Engineer Software Biotech

Indianola, PA · Hybrid

$135K - $155K/yr

Engineer Software Biotech for Indianola, PA to build medical device software for radiology ... Telecommuting permitted from home office location within reasonable commuting distance of Indianola ...

Abbott

Software Compliance Engineer

Alameda, CA · On-site

This person will monitor design controls that govern the development, verification, validation, use, and maintenance of medical device software. The Software Compliance Engineer will also coordinate ...

Abbott

Software Compliance Engineer

Milpitas, CA · On-site

This person will monitor design controls that govern the development, verification, validation, use, and maintenance of medical device software. The Software Compliance Engineer will also coordinate ...

Abbott

Software Compliance Engineer

Milpitas, CA

This person will monitor design controls that govern the development, verification, validation, use, and maintenance of medical device software. The Software Compliance Engineer will also coordinate ...

Werfen

Senior Director, Software Engineering

Norcross, GA

$237K/yr

... based on a clear understanding of market and customer needs for the Technology Center and ... Subject matter expert on national and international medical device software development standards ...

New

Abbott

Software Compliance Engineer

Alameda, CA · On-site

This person will monitor design controls that govern the development, verification, validation, use, and maintenance of medical device software. The Software Compliance Engineer will also coordinate ...

Werfen

Senior Director, Software Engineering

Norcross, GA · On-site

$237K/yr

... based on a clear understanding of market and customer needs for the Technology Center and ... Subject matter expert on national and international medical device software development standards ...

New

Fluxergy

Software Engineer III - Backend

Irvine, CA · On-site

Our product: About the Role As a Software Engineer - Backend, you will be part of an expanding ... Design, develop, and maintain backend applications, APIs, and integrations for our medical device ...

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All JobsHome Based Medical Device Software Engineer Jobs

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 Jul 15, 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 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.
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
Senior Software Business Analyst - Medical Device (Hybrid - Maple Grove, MN) - Contract

Senior Software Business Analyst - Medical Device (Hybrid - Maple Grove, MN) - Contract

Pharmavise

Maple Grove, MN • On-site

$94K - $122K/yr

Contractor

Re-posted 14 days ago

Job description


Our Fortune 500 Medical Device client has an exciting opportunity for a Senior Software Business Analyst.
Job Summary:
We are seeking an experienced Senior Software Business Analyst to join our dynamic team in the medical device industry. This role is critical to bridging the gap between clinical users, business stakeholders, and software development teams. The ideal candidate will possess strong analytical skills, in-depth knowledge of software development practices, and a deep understanding of regulatory and compliance requirements specific to healthcare and medical device software (e.g., FDA, ISO 13485, IEC 62304).
Responsibilities:
• Collaborate with cross-functional teams including product managers, engineers, QA, regulatory, and clinical experts to define software requirements for medical device products.
• Elicit, document, and manage business and functional requirements using industry-standard techniques (e.g., user stories, use cases, process flows).
• Translate complex clinical and business needs into detailed software requirements specifications (SRS).
• Act as the primary liaison between business stakeholders and development teams throughout the product lifecycle.
• Ensure software solutions align with regulatory standards and risk management processes (e.g., design control, traceability, usability).
• Support software validation and verification efforts by reviewing test plans and ensuring requirements coverage.
• Contribute to continuous improvement initiatives within the software development and requirements management processes.
• Facilitate requirement change management processes and impact analysis.
• Participate in audits and regulatory submissions as needed.
Qualifications:
• Bachelor's or Master's degree in Business, Engineering, Computer Science, Biomedical Engineering, or related field.
• 5+ years of experience as a Business Analyst, including at least 2 years in a senior or lead role.
• Proven experience in the medical device industry or regulated healthcare software environment.
• Strong knowledge of IEC 62304, ISO 13485, 21 CFR Part 11, and FDA Design Controls.
• Solid understanding of Agile, Scrum, and/or Waterfall methodologies.
• Proficiency with tools such as Jira, Confluence, Azure DevOps, and requirements management software such as Jama (highly preferred)
• Exceptional communication skills with the ability to convey technical concepts to non-technical stakeholders.
• Strong analytical mindset and attention to detail.
Preferred Qualifications
• Experience with SaMD (Software as a Medical Device) or embedded systems.
• Familiarity with HL7, FHIR, DICOM, or other healthcare interoperability standards.
• Certification such as CBAP, PMI-PBA, or similar is a plus.
Why Join Us?
Work with cutting-edge medical technologies that improve patient outcomes. Collaborate with world-class professionals in a mission-driven organization focused on innovation, compliance, and quality.
Other Details:
• Schedule: 08:00:AM - 04:30:PM CST
• Work Setup: Hybrid at Maple Grove, MN
• Contract Length: 6 Months
• Start Date:9/2/2025

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