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Medical Device Research And Development Jobs in Raleigh, NC

Teleflex

Sr. Engineer, Software Dev, R&D

Morrisville, NC · On-site

$114K - $151K/yr

Principal Responsibilities Lead the development of software for connected medical device software ... Design and develop medical device software that is high quality, safe, secure and compliant. Lead ...

Teleflex

Sr. Engineer, Software Dev, R&D

Morrisville, NC · On-site

$114K - $151K/yr

This role involves providing software leadership for the development and sustainment of medical device software solutions. You will be responsible for delivering high-quality software solutions that ...

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All JobsMedical Device Research And Development JobsMedical Device Research And Development Jobs in Raleigh, NC

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 Aug 22, 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 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 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 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 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:

Medical Device Research And Development jobs near you
Infographic showing various Medical Device Research And Development job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $98,952 per year, or $47.6 per hour.

Director of Research & Development

Valid8 Financial, Inc.

Cary, NC • On-site

$170 - $230/hr

Other

Posted 12 days ago

Job description

VQ Biomedical, based in the Research Triangle Park area of North Carolina, is an early-stage medical device company developing an innovative central venous catheter that delivers oxygen directly to the bloodstream in critically ill ICU patients suffering from lung injury and respiratory failure. VQ is developing the first minimally invasive alternative to mechanical ventilation and ECMO (extracorporeal membrane oxygenation) capable of delivering supplemental oxygen independent of the injured lungs, allowing them to rest, heal, and recover.

Position Summary

The Director of R&D plays a vital role in the leadership of the company. This person will craft and execute R&D strategy, build and lead the R&D team, and drive complex device development from concept through benchtop and preclinical testing and into early clinical evaluation, while ensuring FDA and ISO compliance throughout. This is a hands-on, early-phase role that pairs bench-level engineering with technical leadership. This is a full-time, in-person position that reports to the CEO.

Duties and Responsibilities
  • Develop and execute the R&D strategy and technical roadmap in support of the company’s development and regulatory milestones
  • Build, mentor, and directly manage the R&D team as the company scales
  • Lead the hands-on design, prototyping, and iteration of the oxygenation catheter and its components
  • Develop and execute benchtop testing to characterize and verify device performance
  • Own technical requirements, design inputs and outputs, and verification and validation planning as the design matures
  • Lead risk management activities, including risk analyses and mitigation, in accordance with ISO 14971
  • Establish and maintain the Design History File and supporting quality documentation for new designs and revisions to existing designs
  • Plan, execute, and support preclinical (in vivo) studies in partnership with contract research organizations and clinical experts, and translate findings into design improvements
  • Work cross-functionally with contract manufacturers to build prototypes, develop processes, and establish pilot manufacturing for new products
  • Partner with QA/RA to ensure all R&D activities adhere to ISO 13485, FDA 21 CFR Part 820, and GMP standards
  • Develop schedule and budget estimates, and take responsibility for achieving technical milestones on schedule and on budget
  • Support technical reporting and deliverables for federal grants and contracts
  • Other duties as directed
Skills / Qualifications
  • Bachelor’s or Master’s degree in engineering (biomedical, mechanical, or related field)
  • Minimum of 10 years of relevant medical device product development experience, preferably in a fast-paced small business or startup environment
  • Proven experience in medical device design, specifically catheter design and construction
  • Experience developing and documenting designs within an established, FDA-compliant quality system, including design controls, ISO 13485, and ISO 14971
  • Experience developing benchtop test methods and characterizing device performance
  • Experience planning and supporting preclinical or animal studies
  • Experience starting new manufacturing lines for new products
  • Familiarity with government contract and grant reporting
  • Proficiency with CAD
  • Ability to work in a fast-paced environment and work additional hours as required
  • Ability to adapt to a changing environment and identify and solve problems efficiently
  • Prior experience in a startup environment is a plus
  • Must be able to meet hospital credentialing requirements in order to observe products within a hospital environment

VQ Biomedical is interested in every qualified candidate who is eligible to work in the United States. However, we are not able to sponsor visas.

VQ Biomedical is an equal opportunity employer. As such, we provide employment opportunities without regard to race, color, religion, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, military service, or other characteristics protected by law.

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