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Medical Device Research And Development Jobs (NOW HIRING)

This position is ideal for candidates with hands-on experience in pharmaceutical or medical device R&D who are looking to expand into program management and build capabilities in integrated planning ...

This position is ideal for candidates with hands-on experience in pharmaceutical or medical device R&D who are looking to expand into program management and build capabilities in integrated planning ...

Lead CdTe photovoltaic absorber research and development. * Develop and deploy new manufacturable ... D.) in a Device Development, Process Integration, or Process Development. * Semiconductor / Thin ...

Device Research Manager

Perrysburg, OH ยท On-site

$131K - $187K/yr

Lead CdTe photovoltaic absorber research and development. * Develop and deploy new manufacturable ... D.) in a Device Development, Process Integration, or Process Development. * Semiconductor / Thin ...

DEKA Research & Development, located in Manchester, NH, is seeking a Senior Test Engineer to work in a dynamic medical device R&D environment. This is a high visibility role with a direct impact on ...

R&D Project Manager

Aliso Viejo, CA ยท On-site

$95K - $110K/yr

This position is ideal for candidates with hands-on experience in pharmaceutical or medical device R&D who are looking to expand into program management and build capabilities in integrated planning ...

Conduct research, data analysis, and benchmarking to support client engagements in pharmaceutical, biotech, and medical device R&D * Assist in developing recommendations for process improvements ...

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Medical Device Research And Development information

See salary details

$48.5K

$101.8K

$165K

How much do medical device research and development jobs pay per year?

As of Jul 16, 2026, the average yearly pay for medical device research and development in the United States is $101,794.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,500.00 and $116,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in Medical Device Research and Development, and why are they important?

To thrive in Medical Device Research and Development, you need a solid background in engineering or life sciences, along with experience in product design and knowledge of regulatory standards. Familiarity with CAD software, prototyping tools, and compliance systems such as ISO 13485 or FDA regulations is typically required. Strong problem-solving skills, creativity, and effective teamwork set standout professionals apart in this field. These skills and qualities are crucial to ensure innovative, safe, and compliant medical devices that meet both clinical needs and regulatory requirements.

What are some typical challenges faced by professionals in Medical Device Research and Development, and how can these be managed?

Professionals in Medical Device Research and Development often encounter challenges such as navigating complex regulatory requirements, balancing innovation with safety, and coordinating cross-functional teams. Managing these challenges involves staying current with FDA and international regulations, fostering open communication between engineering, clinical, and regulatory teams, and maintaining rigorous documentation throughout the development process. Strong project management skills and a collaborative mindset are key to overcoming these obstacles and ensuring successful product development.

What is medical device research and development?

Medical device research and development (R&D) is the process of designing, creating, testing, and improving medical devices used for diagnosing, treating, or preventing health conditions. This field combines engineering, biology, and medicine to develop innovative tools ranging from simple instruments to complex implantable devices. Professionals in this area work on everything from concept development and prototyping to clinical trials and regulatory approval. Their work ensures that medical devices are safe, effective, and meet strict regulatory standards before reaching patients.

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

AspectMedical Device Research And DevelopmentMedical Device Quality Assurance
CredentialsEngineering degrees, certifications in R&DQuality certifications, regulatory training
Work EnvironmentLabs, design teams, product developmentInspection facilities, compliance departments
Employer & Industry UsageManufacturers, biotech firms, innovation labsRegulatory agencies, manufacturing companies
Search & Comparison IntentInnovation, product development, prototypingCompliance, testing, product validation

Medical Device Research And Development focuses on designing and developing new medical devices, emphasizing innovation and prototyping. In contrast, Medical Device Quality Assurance ensures products meet safety and regulatory standards through testing and compliance. Both roles are essential in the medical device industry but serve different stages of the product lifecycle.

More about Medical Device Research And Development jobs
What cities are hiring for Medical Device Research And Development jobs? Cities with the most Medical Device Research And Development job openings:
What states have the most Medical Device Research And Development jobs? States with the most job openings for Medical Device Research And Development jobs include:
Infographic showing various Medical Device Research And Development job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 73% Full Time, 21% Part Time, 1% Temporary, and 4% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $101,794 per year, or $48.9 per hour.
Postdoctoral Research Scientist - Industry Medical Device R&D

Postdoctoral Research Scientist - Industry Medical Device R&D

Levisonics, Inc.

Fishers, IN โ€ข On-site

Full-time

Medical, Dental, Vision, PTO

Re-posted 27 days ago


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