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Biomedical Software Engineer Jobs in Indiana (NOW HIRING)

Merican

Systems Designer

Warsaw, IN · On-site +1

Candidates must have experience with software as a medical device (SaMD). Duties and ... Bachelor's degree in engineering or science related field; biomedical engineering preferred.

Johnson & Johnson

Sr. Data Scientist

Warsaw, IN · On-site

Epidemiology, Biomedical Engineering, Data Science, Biostatistics, Applied Statistics, Business ... software technology is required. * Experience cleaning and summarizing large data sets is required.

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Biomedical Software Engineer information

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$60.4K

$140.4K

$195.5K

How much do biomedical software engineer jobs pay per year?

As of May 31, 2026, the average yearly pay for biomedical software engineer in Indiana is $140,378.00, according to ZipRecruiter salary data. Most workers in this role earn between $114,200.00 and $164,600.00 per year, depending on experience, location, and employer.

What is a Biomedical Software Engineer job?

A Biomedical Software Engineer develops software solutions for medical and healthcare applications, including medical devices, diagnostic tools, and research simulations. They combine biomedical knowledge with software development skills to create and maintain systems that improve patient care, enhance medical research, and ensure regulatory compliance. Their work often involves programming, data analysis, and collaboration with healthcare professionals and researchers.

What are the key skills and qualifications needed to thrive in the Biomedical Software Engineer position, and why are they important?

To thrive as a Biomedical Software Engineer, you need a strong background in computer science, biomedical engineering, and software development—often supported by a bachelor's or master's degree in a related field. Proficiency with programming languages such as Python, C++, or Java, familiarity with medical imaging tools, and experience working with healthcare interoperability standards like HL7 or DICOM are typically required. Effective communication, teamwork, and problem-solving skills are crucial for collaborating with cross-functional teams and understanding user requirements. These competencies ensure that biomedical software solutions are safe, compliant, and meet the complex needs of healthcare environments.

What are some typical projects or responsibilities for a Biomedical Software Engineer?

Biomedical Software Engineers often work on designing, developing, and maintaining software used in medical devices, clinical diagnostics, or healthcare information systems. Typical responsibilities include coding new features, troubleshooting and resolving software issues, ensuring compliance with medical standards, and participating in quality assurance testing. You may also collaborate closely with clinicians, researchers, and regulatory specialists to align technological solutions with user needs and safety requirements. These projects frequently involve iterative development and rigorous validation to ensure reliability in real-world medical settings.
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Biomedical Software Engineer jobs near you
Infographic showing various Biomedical Software Engineer job openings in Indiana as of May 2026, with employment types broken down into 1% As Needed, 31% Full Time, 27% Part Time, 2% Temporary, and 39% Contract. Highlights an 100% Physical job distribution, with an average salary of $140,378 per year, or $67.5 per hour.
Systems Designer

Systems Designer

Merican

Warsaw, IN • On-site, Remote

Other

This job post has expired today. Applications are no longer accepted.

Job description

Overview:
TekWissen Group is a workforce management provider throughout the USA and many other countries in the world. Client is a publicly traded medical device company. Client designs, develops, manufactures and markets orthopedics products, including knee, hip, shoulder, elbow, foot and ankle artificial joints and dental prostheses. client has operations in more than 40 countries around the world
Job Title: Systems Designer
Work Location: Warsaw, Indiana 46580
Duration: 7 Months
Job Type: Temporary Assignment
Work Type: Onsite
Job Description:
  • The ideal candidate will have a solid background in medical device design controls and product development, with direct experience in regulatory compliance and documentation. You'll play a key role in refining existing documentation and ensuring continued regulatory alignment to support new and existing products.
  • Candidates must have experience with software as a medical device (SaMD).

Duties and Responsibilities
System Design
  • Define the design approach, ensuring alignment with product objectives, user needs, clinical workflows, and system performance.
  • Translate user needs and system requirements into practical design solutions.
  • Lead design discussions and technical reviews, evaluating alternatives and trade-offs.
  • Ensure design decisions address usability, risk mitigation, technical feasibility, and long-term product sustainability.

System Testing
  • Implement and review product verification and validation (V&V) testing, including developing protocols, test methods, and performance specifications.
  • Perform manual and automated testing and document results accurately.

Product Documentation
  • Collaborate with QA, Service, Compliance, and Regulatory teams to meet documentation requirements and ensure cross-functional alignment.
  • Create, review, and maintain risk management files, including cybersecurity risks.
  • Ensure all product requirements are documented, traceable to verifiable tests, and kept up-to-date.
  • Ensure compliance with FDA, ISO, and internal design controls.
  • Maintain the Design History File (DHF) to be complete, accurate, and regulatory-compliant, addressing gaps proactively.

Requirements
  • 5+ years of experience
  • Strong Experience with Software as a Medical Device (SaMD)
  • Strong experience in design controls in a multi-disciplinary organization.
  • Experience drafting and maintaining DHF (design history file) content, including user needs, design inputs, design outputs, traceability matrices, and risk documentation.
  • Able to support risk analysis (e.g. uFMEA, etc.) and contribute to usability planning and design mitigations.
  • Familiarity with ISO 14971 is required, and IEC 62366 preferred.
  • Ability to define testable requirements, support V&V protocol development, and ensure traceability in collaboration with the Product Development team.
  • Strong collaboration skills across R&D, QA, clinical, and regulatory functions; able to clearly translate technical information across stakeholders.
  • Must have experience in a regulatory environment with strict compliance.
  • Strong analytical skills and accurate judgment-making skills.
  • Ability to deal effectively with internal and external collaborators.
  • Excellent communications skills; written and verbal.
  • Experience with Codebeamer, Jira, or similar.

Education Requirements
  • Bachelor's degree in engineering or science related field; biomedical engineering preferred.

TekWissen® Group is an equal opportunity employer supporting workforce diversity.
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About Merican

Sourced by ZipRecruiter

Merican is a IT Service consulting firm, specialized in Digital adoption and Business automation. With our diverse collection of skilled and committed consultants, technology companies, businesses and digital experts, we provide our subject expertise and our unique client service approach, a best-in-class global model of delivery suited to the business demands of our clients. We ensure that we implement future-oriented solutions for our clients via investments in people, solutions, technologies, competencies and infrastructure.

Industry

It services

Company size

51 - 200 Employees

Headquarters location

Columbia , MD, US

Year founded

2020

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