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Medical Device Research And Development Jobs in Raleigh, NC

Our R&D colleagues are motivated by meaningful impact, energized by teamwork, and skilled at ... Oversee the endtoend lifecycle of a software medical device product from discovery through ...

Senior Device Quality Engineer

Zebulon, NC · On-site

$75K - $101K/yr

... development to post-market surveillance for medical devices within combination products ... Monitor and trend site KPIs for device processes, identify risks, and support development of ...

Senior Device Quality Engineer

Zebulon, NC · On-site

$75K - $101K/yr

... development to post-market surveillance for medical devices within combination products ... Monitor and trend site KPIs for device processes, identify risks, and support development of ...

... research and development. Our history includes the development of many innovative medicines ... This role ensures that medical device complaints are consistently captured, appropriately triaged ...

... research and development. Our history includes the development of many innovative medicines ... This role ensures that medical device complaints are consistently captured, appropriately triaged ...

Product Security Engineer

Morrisville, NC · On-site

$106K - $146K/yr

... medical device products. Partnering with cross-functional teams including Information Security, Regulatory Affairs, Quality Assurance, and Product R&D, you will provide security expertise, risk ...

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Showing results 1-20

Medical Device Research And Development information

See Raleigh, NC salary details

$47.1K

$99K

$160.4K

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 Raleigh, NC is $98,952.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,300.00 and $113,200.00 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.

What are popular job titles related to Medical Device Research And Development jobs in Raleigh, NC? For Medical Device Research And Development jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Medical Device Research And Development jobs in Raleigh, NC look for? The top searched job categories for Medical Device Research And Development jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Medical Device Research And Development jobs? Cities near Raleigh, NC with the most Medical Device Research And Development job openings:
Pr. Engineer, Software Dev, R&D

Pr. Engineer, Software Dev, R&D

Teleflex

Morrisville, NC • On-site

Full-time

Posted 22 days ago


Teleflex rating

8.2

Company rating: 8.2 out of 10

Based on 26 frontline employees who took The Breakroom Quiz


Job description

Expected Travel: Up to 10%
Requisition ID: 14010
About Teleflex Incorporated
As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people's lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare.
Teleflex is the home of Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ - trusted brands united by a common sense of purpose.
At Teleflex, we are empowering the future of healthcare. For more information, please visit teleflex.com.
Vascular & Emergency Medicine - Built on a legacy of innovation and clinical excellence, the Vascular & Emergency Medicine business at Teleflex develops and delivers advanced medical technologies that empower clinicians to help improve patient outcomes and optimize healthcare efficiency. Our trusted Arrow™, Arrow™, EZ-IO™, and QuikClot™ brands set the standard for vascular access and emergency medicine, offering proven solutions to enhance patient outcomes. From technically advanced vascular access devices - including central venous and arterial catheters, PICCs, and sheath introducers with antimicrobial protection-to life-saving intraosseous access systems and hemostatic technologies used by hospitals, EMS, and military teams worldwide, our portfolio embodies precision, reliability, and performance. As part of a high-performing, purpose-driven organization, we are united by a commitment to clinical differentiation, innovation, and excellence. Join a dynamic, growth-focused team that offers advanced medical technology solutions that make a lasting impact on healthcare.
Position Summary
As a Principal Engineer specializing in Software, you will lead technological innovations in vascular positioning systems, including artificial intelligence/machine learning (AI/ML), application software, and embedded software systems. This role involves providing strategic cross-functional technical leadership to ensure alignment with best practices and frameworks for delivering high-quality software solutions. You will be responsible for driving software excellence, achieving reliable and predictable software market releases.
Principal Responsibilities
• Create the overall product software architecture for connected medical device software systems, ensuring scalability, reliability, and maintainability.
• Owns the software development life cycle for connected medical device software systems, ensuring high-quality software is developed that is safe, secure and compliant.
• Lead software developers, third-party designers, vendors, and contractors to deliver high-quality software solutions.
• Lead design control activities and documentation efforts, including requirements, risk assessments and mitigation, traceability, V&V protocols and reports, coding reviews, and software releases.
• Lead and establish software development best practices within a growing business franchise.
• Oversee the end-to-end delivery process of our applications, ensuring smooth and efficient operations from initial planning through development, testing, and deployment of software features.
• Comply with Teleflex's code of Ethics, the company's Quality System, and all company policies, rules, and housekeeping standards.
Education / Experience Requirements
• Bachelors Degree in Computer Science or equivalent with appropriate experience (Computer Engineering, Electrical Engineering).
• 12+ years of software development in senior development and lead roles, preferably in medical devices or regulated industry, with a proven track record of deployment in commercial products.
Specialized Skills / Other Requirements
• Expertise and depth of understanding of modern programming languages (C++ and C#) and design patterns utilized within embedded systems applications.
• Expertise and experience developing medical devices within a Linux environment.
• Expertise and depth of understanding of creating software architecture for Software in Medical Device (SiMD) and Software as Medical Device (SaMD) software systems.
• Knowledge and experience with Cybersecurity best practices and Cybersecurity compliance as it pertains to FDA guidance within the development of medical devices.
• Experience utilizing an Agile software development framework, including Scrum and Continuous Integration/Delivery (CI/CD).
• Proven experience as a Software Team Leader with the ability to influence and collaborate with key stakeholders and leaders.
• Experience with medical device regulatory standards such as 21 CFR Part 820, IEC 60601, IEC 62304, and ISO 13485, including experience with system risk, hazard analysis, and DFMEA.
• Deep commitment to understanding and solving problems for end users, with an ability to translate into software requirements, design, and test specifications.
• Highly motivated to develop talent, mentor, and build high-performing teams. Track record of strong cross-functional collaboration, influence without authority, and project management, enabling highly effective project teams.
• Proven self-starter who runs towards critical issues, ambiguous requirements, or loosely defined challenges with a demonstrated ability to rally teams to achieve business results.
• Comfortable debugging complex integrated systems spanning hardware, embedded, and application software in medical devices (preferred).
• Familiarity with ECG monitoring systems and Ultrasound imaging systems (preferred).
• Experience with regulated software incorporating artificial intelligence and machine learning (preferred).
• Experience with software development and workflows incorporating AI-based development tools (preferred).
• Excellent verbal and written communication skills.
#LI-EB1
Working Conditions / Physical Demands
TRAVEL REQUIRED: <10%
WORKING ENVIRONMENT:
☒ Office/Professional ☐ Plant/Manufacturing ☐ Remote/Field ☐ Laboratory
At Teleflex, we follow a comprehensive hiring process. We do not accept unsolicited resumes from agency recruiters or 3rd party firms. We do not make unsolicited job offers. We do not ask for money or require equipment purchase up-front.
Teleflex Incorporated is an equal opportunity employer. Applicants will be considered without regard to age, race, religion, color, national origin, ancestry, sexual orientation, disability, nationality, sex, or veteran status. If you require accommodation to apply for a position, please contact us at: 877-880-8588 or Talent@Teleflex.com.
Teleflex, the Teleflex logo, Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries.
© 2026 Teleflex Incorporated. All rights reserved.

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