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Medical Device Innovation Jobs in Indiana (NOW HIRING)

Nexxt Spine

CNC Mill Setup/Operator

Noblesville, IN · On-site

$20.75 - $27.50/hr

... medical device industry, dedicated to designing, manufacturing, and distributing an expanding portfolio of innovative spinal implants and instruments. We are committed to a culture of innovation ...

Freudenberg

Project Manager

Jeffersonville, IN · On-site

... innovation, and regulatory excellence across the organization. * Manages a few discrete projects ... Understanding of scientific principles and manufacturing processes used in medical device ...

Levisonics Inc

Engineering Project Manager

Fishers, IN · On-site

About Us: We are a dynamic and innovative medical device startup developing a point-of-care ... Operating in a fast-paced startup, we value innovation, adaptability, and proactive mindsets. Ideal ...

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All JobsMedical Device Innovation JobsMedical Device Innovation Jobs in Indiana

Medical Device Innovation information

See Indiana salary details

$20

$47

$91

How much do medical device innovation jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for medical device innovation in Indiana is $47.42, according to ZipRecruiter salary data. Most workers in this role earn between $33.41 and $56.73 per hour, depending on experience, location, and employer.

What is the difference between Medical Device Innovation vs Medical Device Regulatory Affairs?

AspectMedical Device InnovationMedical Device Regulatory Affairs
Primary FocusDeveloping new medical devices, product design, and technological advancementsEnsuring compliance with regulations, managing submissions, and maintaining approval processes
Required CredentialsEngineering, product development, or biomedical backgroundsRegulatory affairs certifications, healthcare law knowledge
Work EnvironmentResearch labs, product development teams, innovation hubsRegulatory agencies, corporate compliance departments
Industry UsageDesign and create innovative medical devicesNavigate regulatory pathways and ensure legal compliance

Medical Device Innovation focuses on creating and developing new medical devices, emphasizing engineering and product design. In contrast, Medical Device Regulatory Affairs concentrates on ensuring that devices meet legal and safety standards, managing approval processes. Both roles are essential in the medical device industry but serve different functions in bringing a product from concept to market.

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

Professionals in Medical Device Innovation often encounter challenges such as navigating complex regulatory requirements, ensuring cross-functional collaboration, and balancing innovation with patient safety. Staying up-to-date with regulatory changes and fostering open communication among engineering, clinical, and regulatory teams are essential for success. Additionally, adopting agile development methodologies and engaging with end-users early in the design process can help address these challenges and lead to more effective, compliant products.

What is medical device innovation?

Medical device innovation refers to the development and improvement of medical instruments, equipment, and technologies used in healthcare to diagnose, treat, or monitor patients. This process involves research, design, prototyping, regulatory approval, and commercialization of new or enhanced medical devices. The goal is to address unmet medical needs, improve patient outcomes, and increase the efficiency of healthcare delivery. Professionals in this field work closely with clinicians, engineers, and regulatory bodies to ensure devices are safe, effective, and compliant with industry standards.

What are the key skills and qualifications needed to thrive in medical device innovation?

To thrive in Medical Device Innovation, you need a strong background in biomedical engineering or related fields, knowledge of regulatory standards, and experience with product development. Familiarity with CAD software, prototyping tools, and regulatory approval processes such as FDA or CE marking is typically required. Creativity, problem-solving, and effective cross-functional communication are standout soft skills in this role. These competencies are essential for designing safe, effective devices that meet market needs and comply with stringent regulations.
What are popular job titles related to Medical Device Innovation jobs in Indiana? For Medical Device Innovation jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Medical Device Innovation jobs in Indiana look for? The top searched job categories for Medical Device Innovation jobs in Indiana are:
Medical Device Innovation jobs near you
Infographic showing various Medical Device Innovation 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 $98,641 per year, or $47.4 per hour.

Embedded Systems Engineer for Medical Device Startup

Levisonics Inc

Fishers, IN • On-site

Full-time

Medical, Dental, Vision, PTO

Re-posted 12 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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