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Junior Medical Device Software Engineer Jobs (NOW HIRING)

Eightelevengroup

Software Quality Engineer

Warsaw, IN · On-site

$76 - $88/hr

Software Quality Engineer Warsaw, IN Hybrid role (3 days in office) $55 - $64 per hour ABOUT THE ... Support the design, development, and testing of medical device software, including Software as a ...

Cesna Group

Senior Software Engineer

San Diego, CA · On-site

$100K - $200K/yr

As medical device development is iterative and subject to regulatory, technical, and business ... junior engineers, conduct code reviews, and promote best practices in software development ...

Ziehm Orthoscan

Senior Software Engineer

Scottsdale, AZ

$123K - $163K/yr

Experience * 7+ years of experience in software engineering, with experience in medical device or ... other regulated or safety-critical environments strongly preferred. * Strong proficiency in ...

Orthoscan, Inc.

Senior Software Engineer

Scottsdale, AZ · On-site

$120 - $170/hr

Experience * 7+ years of experience in software engineering, with experience in medical device or ... other regulated or safety-critical environments strongly preferred. * Strong proficiency in ...

Orthoscan, Inc.

Senior Software Engineer

Scottsdale, AZ · On-site

$123K - $163K/yr

Experience * 7+ years of experience in software engineering, with experience in medical device or ... other regulated or safety-critical environments strongly preferred. * Strong proficiency in ...

Brooksource

Software Quality Engineer

Indianapolis, IN · On-site

$55 - $64/hr

Software Quality Engineer Warsaw, IN Hybrid role (3 days in office) $55 - $64 per hour ABOUT THE ... Support the design, development, and testing of medical device software, including Software as a ...

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Junior Medical Device Software Engineer information

See salary details

$46.5K

$94.5K

$142K

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

As of Sep 3, 2026, the average yearly pay for junior medical device software engineer in the United States is $94,542.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,000.00 and $95,500.00 per year, depending on experience, location, and employer.

What does a junior medical device software engineer do?

A Junior Medical Device Software Engineer assists in designing, developing, testing, and maintaining software for medical devices under the supervision of senior engineers. They help ensure that the software meets regulatory standards for safety and performance. Their work may involve writing code, debugging, documenting processes, and collaborating with cross-functional teams such as hardware engineers and quality assurance. This role is ideal for recent graduates or those with a few years of experience looking to build a career in the intersection of healthcare and technology.

What are the key skills and qualifications needed to thrive as a junior medical device software engineer?

To thrive as a Junior Medical Device Software Engineer, you need a solid background in software development (often with a degree in computer science or biomedical engineering), knowledge of medical device regulations, and familiarity with embedded systems. Experience with programming languages like C/C++, development environments, and compliance with standards such as IEC 62304 are typically required. Attention to detail, problem-solving abilities, and strong teamwork and communication skills help you excel in this role. These competencies are essential to ensure the safe, effective, and compliant development of medical device software in a highly regulated industry.

What are some common challenges faced by junior medical device software engineers in their first year on the job?

Junior Medical Device Software Engineers often encounter challenges such as adapting to strict regulatory standards, learning thorough documentation practices, and understanding the complexities of safety-critical software development. Working in multidisciplinary teams, they must quickly become proficient in both software engineering and medical device compliance, such as FDA or ISO standards. Successfully navigating these challenges requires strong communication skills, attention to detail, and a willingness to learn from senior engineers and cross-functional colleagues.

What is the difference between Junior Medical Device Software Engineer vs Medical Device Software Engineer?

AspectJunior Medical Device Software EngineerMedical Device Software Engineer
Required CredentialsTypically an entry-level degree (BSc or MSc) in Software Engineering, Biomedical Engineering, or related fields; may include basic certificationsSame as junior, but often with more professional experience or advanced certifications
Work EnvironmentSupportive team settings within medical device companies or healthcare tech firmsMore independent roles with increased responsibility in design, testing, and validation
Employer & Industry UsageCommonly used in medical device manufacturing, healthcare technology companies, and startupsUsed across medical device companies, regulatory bodies, and R&D departments

The main difference between a Junior Medical Device Software Engineer and a Medical Device Software Engineer lies in experience and responsibility. Junior roles focus on learning and supporting development tasks, while the more experienced engineer takes on complex design and validation responsibilities.

What cities are hiring for Junior Medical Device Software Engineer jobs?

Cities with the most Junior 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 Junior Medical Device Software Engineer jobs?

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

Junior Medical Device Software Engineer jobs near you
Infographic showing various Junior Medical Device Software Engineer job openings in the United States as of July 2026, with employment types broken down into 77% Full Time, 14% Part Time, and 9% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $94,542 per year, or $45.5 per hour.

Software Quality Engineer

Eightelevengroup

Warsaw, IN • On-site

$76 - $88/hr

Other

Posted 16 days ago

Key responsibilities

  • Support the design, development, and testing of medical device software, including Software as a Medical Device (SaMD) products

  • Review test case execution results and manage software defects

  • Facilitate software risk assessment sessions and own the development of risk documentation

Job description

Software Quality Engineer

Warsaw, IN

Hybrid role (3 days in office)

$55 - $64 per hour

ABOUT THE ROLE

Join a Fortune 50 Life Sciences company as a Software Quality Engineer, providing quality leadership for a new product project team focused on the development of medical device software systems. In this hybrid role based in Warsaw, IN, you will serve as the subject matter expert in requirements gathering, software risk assessments, test strategy definition, and guiding the team on design controls and defect analysis. You will partner closely with R&D throughout the full development lifecycle—from upstream requirements and risk through mid-stream verification to ongoing compliance and audit readiness. This is a high-visibility opportunity to own quality end-to-end, gain exposure to a full medical device software toolchain, and collaborate cross-functionally with business partners and mentors.

WHAT YOU'LL DO
  • Support the design, development, and testing of medical device software, including Software as a Medical Device (SaMD) products
  • Provide leadership, guidance, and expertise on software development processes, procedures, and practices
  • Serve as a subject matter expert in requirements gathering, test strategy definition, and design controls
  • Facilitate documentation and tracking of verification activities, including code review findings
  • Review test case execution results and manage software defects
  • Facilitate software risk assessment sessions and own the development of risk documentation
  • Support regulatory filings and registrations, including 510(k) submissions and Design History File (DHF) creation
  • Provide technical support for audits of software suppliers and consultants, including cybersecurity and threat modeling topics
  • Conduct training on medical device software development processes and quality systems; develop associated work instructions
  • Provide expertise in applicable industry standards and regulations (e.g., IEC 62304, FDA guidance, FDA Part 11, ISO 13485, EU MDR, ISO 14971, IEC 62366, ISO 27001, HIPAA)
  • Collaborate closely with R&D and cross-functional teams to ensure compliance with industry standards and regulatory requirements
WHAT YOU BRING
  • Bachelor's degree or university degree in Engineering, Computer Science, Information Systems, or Biomedical/Bio-engineering (required)
  • Minimum 4 years of regulated industry experience in quality, new product development, or manufacturing engineering
  • Experience in the medical device industry
  • Proficiency with quality tools, systems, and processes (e.g., Windchill, Polarion, ETQ)
  • Strong interpersonal, organizational, and verbal/written communication skills
  • Ability to work collaboratively in a team environment and demonstrate leadership
  • Ability to perform duties in accordance with company policies, procedures, and civil rights requirements
  • ASQ Certification as a Software Quality Engineer or equivalent (preferred)
  • Expertise in applicable industry standards and regulations (e.g., IEC 62304, FDA guidance, FDA Part 11, ISO 13485, EU MDR, ISO 14971, IEC 62366, ISO 27001, HIPAA)
  • Experience supporting regulatory filings and registrations (e.g., 510(k) submissions, DHF creation)
  • Ability to facilitate software risk assessments and develop risk documentation
WHAT'S IN IT FOR YOU
  • Opportunity to own quality end-to-end on a high-visibility project for a Fortune 50 Life Sciences company
  • Exposure to a full medical device software toolchain (Windchill, Polarion, ETQ) and hands-on involvement
  • Meaningful mentorship scope and cross-collaborative team and business partners
  • Hybrid work environment (3 days in office)
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