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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 ...

Stellent IT LLC

Sr. Statistician//W2

Bloomington, IN · On-site

$75K - $93K/yr

... medical device development and manufacturing. The Sr. Statistician will join a small but talented statistical consulting team and partner with engineering, quality, production, and technical teams to ...

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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 Jun 30, 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.
What are popular job titles related to Medical Device Development jobs in Indiana? For Medical Device Development jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Medical Device Development jobs in Indiana look for? The top searched job categories for Medical Device Development jobs in Indiana are:
Medical Device Development jobs near you
Postdoctoral Research Scientist - Industry Medical Device R&D

Postdoctoral Research Scientist - Industry Medical Device R&D

Levisonics, Inc.

Fishers, IN • On-site

Full-time

Medical, Dental, Vision, PTO

Posted 12 days ago

Key responsibilities

  • Develop and implement research plans using proprietary diagnostic prototypes to investigate blood coagulation dynamics.

  • Design and execute experimental studies, analyze research data, and interpret results to generate actionable insights.

  • Contribute significantly to the preparation of grant applications and communicate research outcomes through reports and publications.

Job description

About Us:
We are a dynamic and innovative medical device startup developing a point-of-care blood coagulation testing device. Our fast-growing team is passionate about transforming diagnostic testing and improving patient care. As a small, mission-driven company, we offer a collaborative environment where team members can take ownership, contribute meaningfully, and grow with us. We're looking for versatile, motivated individuals who are excited to be part of an early-stage team and make a real-world impact.
Job Summary:
We're seeking a Postdoctoral Research Scientist with a strong background in coagulation, diagnostics, and experimental research to join our core R&D team. This is a unique opportunity to contribute to the advancement of next-generation diagnostic technology in a hands-on, high-growth startup environment. The ideal candidate will bring deep scientific knowledge, creativity in study design, strong data analysis skills, and an entrepreneurial mindset.
You'll play a critical role in shaping and executing research projects, designing and running experiments, interpreting data, identifying grant opportunities, and contributing to scientific writing for grant proposals and publications. This position is ideal for someone who thrives in a fast-paced environment, loves solving hard problems, and is excited about translating scientific insight into life-changing technology.
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 making a meaningful impact in the medical device industry and are excited to tackle challenges head-on.
Key Responsibilities:
  • Develop and implement research plans using Levisonics' proprietary diagnostic prototypes to investigate blood coagulation dynamics.
  • Design and execute experimental studies, including study planning, hypothesis generation, and experimental protocol development.
  • Conduct literature reviews to support experimental design, regulatory documentation, and ongoing product development.
  • Optimize protocols for accuracy, reproducibility, and compliance with ethical and regulatory standards.
  • Acquire and analyze research data using statistical and bioinformatics tools; identify trends, patterns, and correlations.
  • Visualize and interpret data to generate actionable insights and guide prototype improvements.
  • Collaborate closely with internal engineers, external clinicians, and research partners to align scientific and technical goals.
  • Identify and evaluate relevant grant opportunities (e.g., NIH, NSF, DoD) and contribute significantly to the preparation of competitive grant applications, including Specific Aims, Research Strategy, and biosketches.
  • Communicate research outcomes clearly through reports, internal presentations, publications, and regulatory materials.
  • Contribute to the continuous improvement of prototype functionality and experimental capabilities.
  • Support cross-functional needs and take on ad-hoc tasks typical of a startup environment.

Minimum Qualifications:
  • Ph.D. in Medical Sciences, Biomedical Engineering, Bioengineering, or a related field.
  • Strong independent R&D experience, ideally in coagulation, hematology, trauma, or diagnostic technologies.
  • Proven ability to design, execute, and interpret experiments.
  • Proficiency with data analysis and visualization tools (Python, R, MATLAB, GraphPad, etc.).
  • Strong scientific writing and literature review skills.
  • Experience in identifying and writing grant applications.
  • Prior experience with diagnostic or point-of-care device development is a plus.
  • Strong communication and teamwork skills.
  • Entrepreneurial mindset and ability to adapt in a fast-paced, evolving environment.
  • Publication record in peer-reviewed journals.

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

Apply