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Medical Device Development Jobs in Indiana (NOW HIRING)

Imh

Patient-specific biomedical technology development * Visceral anatomy segmentation and quantitative assessment * Complex anatomy Reconstruction * Patient specific Medical Device Design * CFD and ...

Techlink Systems

Be Seen First

Assembler - Cleanroom/Medical Device - RM26

Westfield, IN · On-site

$20 - $21.65/hr

... related medical device assemblies. Performs routine assignments according to specified and/or ... development and support centers globally. We are a MBE (NMSDC), WBE (WBENC), and WOSB certified ...

New

BSI Prof Serv EHS West

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 ...

BSI Group

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 ...

Prophecy Technologies

Quality Engineer

Indianapolis, IN · 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 ...

Zimmer, Inc.

Development Engineer II

Warsaw, IN · On-site

What You Can Expect As Development Engineer II, you have a key support role with expanded ... FDA QSR and EU MDR medical device regulatory requirements, and industry/ regulatory body recognized ...

BSI Group

As a Technical Reviewer, you will work with medical device manufacturers throughout their ... and development. The salary for this position for the UK can range from 58,500- 78,000 annually ...

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Showing results 21-40

All JobsMedical Device Development JobsMedical Device Development Jobs in Indiana

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 Aug 14, 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 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 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.

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 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.
Medical Device Development jobs near you
Infographic showing various Medical Device Development job openings in Indiana as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 16% Part Time, and 6% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $50,830 per year, or $24.4 per hour.

Embedded Systems Engineer for Medical Device Startup

Levisonics Inc

Fishers, IN • On-site

Full-time

Medical, Dental, Vision, PTO

Re-posted 14 days ago

Job description

About Us: We are a dynamic and innovative medical device startup developing a point-of-care portable blood coagulation testing device.

Job Summary: We are seeking a talented and experienced Embedded Systems Engineer to join our team and lead the design and development of embedded computing systems, guiding our devices from prototypes to commercial readiness. The ideal candidate will have a Bachelor's or Master’s degree in Electrical Engineering, Computer Engineering, or a related field, with at least 5 years of experience (Ph.D. preferred). You will drive embedded hardware/software development for real-time systems, emphasizing proficiency in C, C++, and/or assembly language for hardware interfacing and optimization. Experience in hardware architectures, sensors, actuators, and communication protocols is crucial, alongside a knack for evaluating and selecting optimal components. Hands-on experience with embedded processors and display integration, as well as a strong grasp of design modification processes to enhance device durability, are also required. Proficiency in coding and optimizing for resource-constrained environments is a plus. As the first embedded engineer on our team, you will play a pivotal role in advancing our blood coagulation testing device from prototype to production. This role is critical to the success of our product and involves working on multiple federal grants and projects. You will be responsible for both hardware and software components, ensuring our device is efficient, reliable, and ready for market.

Startup Environment: Operating in a fast-paced startup, we value innovation, adaptability, and proactive mindsets. Ideal team members thrive under pressure, manage multiple projects, and adapt as company needs evolve. 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. 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. Design & build portable battery system for power supply.
  2. Improve sample handling system design.
  3. Implement an independent embedded processing system and streamlined user interface for straightforward operation.
  4. Upgrade embedded processing system.
  5. Develop efficient injection/fluid handling systems.
  6. Identify and implement efficient computing by selecting and implementing embedded computers to run inside the medical device.
  7. Ensure the embedded system replaces the laptop.
  8. Integrate various hardware and software components together.
  9. Enable battery operation of the device.
  10. Design and develop sample handling systems and cartridges.
  11. Lead end-to-end projects for multiple federal grants and develop innovative solutions.
  12. Collaborate with other team members in taking device prototypes to market.
  13. Participate in FDA-related activities and follow quality protocols.
  14. Participate in grant writing or other fundraising activities as needed.
  15. Perform other relevant tasks as needed for the company.

Minimum Qualifications:

  • Bachelors in Electrical Engineering, Computer Engineering, or a related field and minimum 5 years of experience.
  • Proven experience in embedded systems engineering, preferably in the medical device industry.
  • Knowledge of sensors and commercial medical devices.
  • Proficiency in C, C++, and/or assembly language for embedded software development.
  • Experience with battery systems, fluid handling systems, and embedded processing systems.
  • Familiarity with CAD design, particularly using software like SolidWorks.
  • Understanding of calibration techniques.
  • Familiarity with injection molding and 3D printing for rapid prototyping.
  • Ability to design devices for manufacturing at scale.
  • Knowledge of cybersecurity as it relates to medical devices.
  • Familiarity with rheology/acoustics topics is a plus.
  • Strong problem-solving and analytical skills.
  • Ability to learn new concepts proactively and break down work effectively.
  • Familiarity with Agile methodologies and efficient project management.
  • Demonstrated accountability, effective planning, and team leadership.
  • Innovative thinker with a track record of generating new ideas.
  • Strong written and verbal communication skills.

Preferred Qualifications:

  • Masters or Ph.D. in Electrical Engineering, Computer Engineering, or a related field.
  • Experience selecting and implementing embedded processors and displays.
  • Prior startup or medical device development experience
  • Experience in medical device 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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