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Freelance Medical Device Software Engineer Jobs (NOW HIRING)

Senior SQA Engineer

Natick, MA · On-site

$120K - $130K/yr

Senior SQA Engineer Department: Product Development Reports To: Principal SQA Engineer/Tech Lead ... Develop solid understanding of the medical device software products * Document testing ...

Senior SQA Engineer

Natick, MA · On-site

$120K - $130K/yr

Senior SQA Engineer Department: Product Development Reports To: Principal SQA Engineer/Tech Lead ... Develop solid understanding of the medical device software products * Document testing ...

Senior Software Engineer

San Diego, CA · On-site

$100K - $200K/yr

We are seeking a Senior Software Engineer to play a key role in maintaining, evolving, and ... As medical device development is iterative and subject to regulatory, technical, and business ...

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Freelance Medical Device Software Engineer information

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$14

$47

$132

How much do freelance medical device software engineer jobs pay per hour?

As of Jun 25, 2026, the average hourly pay for freelance medical device software engineer in the United States is $47.71, according to ZipRecruiter salary data. Most workers in this role earn between $24.28 and $61.78 per hour, depending on experience, location, and employer.
What are the most commonly searched types of Medical Device Software Engineer jobs? The most popular types of Medical Device Software Engineer jobs are:
Infographic showing various Freelance Medical Device Software Engineer job openings in the United States as of June 2026, with employment types broken down into 3% Locum Tenens, 53% Full Time, 37% Part Time, 1% Contract, and 6% Nights. Highlights an 77% Physical, 2% Hybrid, and 21% Remote job distribution, with an average salary of $99,230 per year, or $47.7 per hour.

Software Verification and Validation Engineer

Futran Tech Solutions Pvt. Ltd.

Goleta, CA • On-site

Full-time

Posted 5 days ago


Job description

Role: Software Verification and Validation Engineer
Customer: Alcon; Location: Goleta, California
Remote Work: No
Job Description
Bachelor or master's degree in computer science or Equivalent
10+ years' Experience in Software Engineering Development Process (SEDP) which compliance with IEC 62304
Creating Computerized Systems Validation (CSV) reports and submissions for SW tools used in our V+V process, including SW simulators, key generators, language translation tools, etc.
Develop validation and test procedures for updating software components, including the base operating system, compliant with the Alcon SEDP. This will require close collaboration with the engineers developing this system.
Review and update SW Development and Test plans to ensure they align with our development practices and properly satisfy the Alcon QMS requirements
Prepare for and participate Design Output reviews, supporting the engineering team, including submissions to Windchill.
Medical device experience is must
Skill Set Yes / No No. of Years' Experience Remarks
*Experience in Software Engineering Development Process (SEDP) which compliance with IEC 62304
*Creating Computerized Systems Validation (CSV) reports for V&V process
*Develop validation and test procedures for updating software components
*Medical device software experience