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Medical Device Development Jobs in Indiana (NOW HIRING)

EMEA/UK- Homebased BSI is seeking R&D Scientists and Production Scientists to join our IVD Devices ... Provide Medical Device QMS assessment and device expertise leadership and mentoring in areas of ...

EMEA/UK- Homebased BSI is seeking R&D Scientists and Production Scientists to join our IVD Devices ... Provide Medical Device QMS assessment and device expertise leadership and mentoring in areas of ...

Join the healthcare information technology team that's turning drug and medical device data into ... Ability to research devices, categories, and HCPCS codes leading to the development of a library.

Join the healthcare information technology team that's turning drug and medical device data into ... Ability to research devices, categories, and HCPCS codes leading to the development of a library.

Join the healthcare information technology team that's turning drug and medical device data into ... Ability to research devices, categories, and HCPCS codes leading to the development of a library.

Join the healthcare information technology team that's turning drug and medical device data into ... Ability to research devices, categories, and HCPCS codes leading to the development of a library.

Join the healthcare information technology team that's turning drug and medical device data into ... Ability to research devices, categories, and HCPCS codes leading to the development of a library.

Join the healthcare information technology team that's turning drug and medical device data into ... Ability to research devices, categories, and HCPCS codes leading to the development of a library.

Join the healthcare information technology team that's turning drug and medical device data into ... Ability to research devices, categories, and HCPCS codes leading to the development of a library.

Development Engineer

Warsaw, IN ยท On-site

$60 - $85/hr

Support the design, development, and commercialization of medical device products. * Develop an understanding of product intended use, clinical procedures, and applicable regulations and industry ...

New

Quality Engineer

Indianapolis, IN ยท On-site

$68K - $88K/yr

* Support Design History File (DHF) activities for medical device development projects. * Review, update, and maintain Global dFMEA documentation ensuring risks are adequately identified, analyzed, and ...

Showing results 21-40

Medical Device Development information

See Indiana salary details

$27.6K

$50.8K

$77.1K

How much do medical device development jobs pay per year?

As of Sep 4, 2026, the average yearly pay for medical device development in Indiana is $50,830.00, according to ZipRecruiter salary data. Most workers in this role earn between $40,400.00 and $57,100.00 per year, depending on experience, location, and employer.

What is medical device development?

Medical device development is the process of designing, creating, testing, and bringing medical devices to market. This process involves multiple stages, including concept development, prototyping, preclinical and clinical testing, regulatory approval, and manufacturing. The goal is to ensure that new devices are safe, effective, and meet regulatory standards before they are used by healthcare professionals or patients. Teams in medical device development often include engineers, scientists, regulatory specialists, and quality assurance professionals.

What are the key skills and qualifications needed to thrive in medical device development, and why are they important?

To thrive in Medical Device Development, you need expertise in engineering or life sciences, a solid understanding of regulatory requirements, and often an advanced degree such as a master's or Ph.D. in a relevant field. Familiarity with CAD software, prototyping tools, and knowledge of FDA or ISO regulatory standards is typically required. Strong problem-solving abilities, collaboration, and effective communication distinguish top professionals in this field. These skills ensure the development of safe, innovative, and compliant medical devices that meet both user needs and regulatory standards.

What are some common challenges faced by professionals in medical device development, and how can they be addressed?

Professionals in medical device development frequently encounter challenges such as navigating complex regulatory requirements, ensuring product safety and efficacy, and managing cross-functional collaboration between engineering, clinical, and regulatory teams. Addressing these challenges requires staying updated on evolving regulations, fostering open communication among diverse team members, and implementing robust quality control processes. Proactively engaging with regulatory bodies and regularly reviewing project milestones can help streamline development and reduce the risk of costly delays.

What is the difference between Medical Device Development vs Medical Device Quality Assurance?

AspectMedical Device DevelopmentMedical Device Quality Assurance
CredentialsEngineering degrees, certifications like RAPS or regulatory trainingQuality certifications, ISO 13485, regulatory compliance training
Work EnvironmentDesign labs, R&D teams, product development settingsManufacturing sites, quality control labs, compliance departments
Industry UsageDesigning and creating new medical devicesEnsuring devices meet quality and regulatory standards

Medical Device Development focuses on designing and creating new medical devices, involving engineering and product innovation. Medical Device Quality Assurance ensures these devices meet safety, quality, and regulatory standards through testing and compliance processes. Both roles are essential in the medical device industry but serve different functions in the product lifecycle.

Infographic showing various Medical Device Development job openings in Indiana as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, and 5% Contract. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $50,830 per year, or $24.4 per hour.

Senior Software Engineer for Medical Device Startup

Levisonics Inc

Fishers, IN โ€ข On-site

$115K - $152K/yr

Full-time

Medical, Dental, Vision, PTO

Re-posted 27 days ago


Key responsibilities

  • Optimize and enhance existing software written in Python to improve efficiency and processing speed, including conversion for embedded devices.

  • Package, secure, and deploy the software, ensuring connectivity to the internet and online databases, while implementing security measures for health data.

  • Develop and convert algorithms and data processing software, create user interfaces, and implement parallel processing and language conversion for optimal performance on embedded hardware.


Job description

About Us: 
We are a dynamic and innovative medical device startup developing a point-of-care portable blood coagulation testing device. Our full-time team currently comprises a CEO/Biomedical Engineer, and an Electrical Engineer. 

Job Summary: 
We are seeking a talented and experienced Senior Software Engineer to join our team and lead the development and optimization of software workflows for our innovative acoustic tweezing technology-based medical devices. The ideal candidate will have a Master's degree in Computer Science, Software Engineering, or a related field, with a minimum of 5 years of experience. This role requires strong coding skills in Python and C/C++, proficiency in developing intuitive and visually engaging graphical user interfaces, and expertise in SQL for effective data management and database design. Experience with version control systems, particularly Git, is essential, along with the ability to understand and generate code from workflow diagrams. As the first and only software engineer on the team, you will play a pivotal role in shaping the software development efforts for our groundbreaking technology. This role is critical to the success of our product and involves working on multiple federal grants and projects. 

Startup Environment: 
We operate in a fast-paced startup environment where innovation, adaptability, and a proactive mindset are key to success. We are looking for individuals who are passionate about working in a startup setting and thrive in dynamic and challenging situations. We value individuals who are not just seeking a job but are driven by a genuine passion for creating impactful solutions and driving change in the medical device industry. Our team members are expected to work well under pressure, juggle multiple projects, and be flexible in their roles as the needs of the company evolve. If you are excited about the opportunity to make a meaningful impact and are ready to roll up your sleeves and tackle challenges head-on, we encourage you to apply. 

Key Responsibilities: 

  1. Optimize and Enhance Existing Software: 

  • Improve the efficiency of our existing software written in Python. 

  • Increase processing speed for short-term operation on laptops. 

  • Convert and optimize the software for embedded computing devices inside the medical device long-term. 

  1. Software Packaging and Security: 

  • Secure the code to prevent reverse engineering. 

  • Package the software into executable files for easy installation and deployment. 

  1. Connectivity and Data Management: 

  • Ensure the software can connect to the internet. 

  • Implement connectivity to an online database for long-term data management. 

  • Incorporate Data Science, Machine Learning, and AI for handling large amounts of health data. 

  1. Health Data Security: 

  • Ensure the highest level of security for software and health data management. 

  1. New Technique Development: 

  • Convert and develop existing crude MATLAB codes and technology algorithms into efficient software for commercial use. 

  • Create executable files with efficient large data handling capabilities. 

  • Develop complex data processing software and manage large data analysis. 

  • Develop a user-friendly interface for healthcare professionals. 

  • Implement a remote kill switch for the software. 

  • Apply all relevant requirements from existing software. 

  1. Parallel Processing and Language Conversion: 

  • Implement efficient parallel processing techniques. 

  • Convert existing Python code to C/C++ or another suitable low-level efficient language to run software optimally on embedded hardware. 

  1. Other Responsibilities: 

  • Develop high-quality, efficient, and maintainable code. 

  • Design intuitive and visually engaging user interfaces. 

  • Proactively take on new responsibilities and suggest innovative ideas for product and company growth. 

  • Participate in grant writing and fundraising activities. 

  • Engage in FDA-related activities and adhere to quality protocols. 

  • Perform other relevant software-related tasks as needed for the company. 

Minimum Qualifications: 

  • Master’s degree in Computer Science, Software Engineering, or a related field. 

  • Minimum of 5 years of experience in software development. 

  • Strong coding skills in Python, C, and C++ (JavaScript is a plus). 

  • Proficiency in developing intuitive and visually engaging graphical user interfaces. 

  • Proficiency in SQL for effective data management and database design. 

  • Experience with version control systems, particularly Git. 

  • Ability to understand and generate code from workflow diagrams. 

  • Knowledge of integrating multiple devices and establishing centralized control. 

  • Familiarity with IDEs, preferably PyCharm. 

  • Excellent problem-solving skills and ability to work independently. 

  • Strong written and verbal communication skills. 

Preferred Qualifications: 

  • Experience working in the medical device industry. 

  • Familiarity with Agile development methodologies. 

  • Knowledge of machine learning techniques and algorithms. 

  • Experience with Docker and containerization technologies. 

  • Familiarity with cloud platforms such as AWS or Azure. 

  • Prior experience working in startups. 

  • Experience with embedded systems and medical device software development. 

  • Strong knowledge of data security, especially related to health data. 

  • Knowledge of parallel processing and algorithm optimization. 

  • Innovative mindset with a track record of proactive contributions. 

  • Experience in grant writing and regulatory compliance (FDA). 

What We Offer: 

  • Competitive salary 

  • Health, dental, and vision insurance coverage 

  • Generous paid time off 

  • Professional development opportunities 

  • Potential to receive stock options 

  • Opportunities for growth within the company 

  • Flexible work arrangements, including remote work options 

  • Dynamic and innovative startup environment 

  • Opportunity to make a meaningful impact in the medical device industry 

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