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Medical Device Product Development Manager Jobs in Raleigh, NC

Teleflex

Sr. Engineer, Software Dev, R&D

Morrisville, NC · On-site

$114K - $151K/yr

Design and develop medical device software that is high quality, safe, secure and compliant. Lead ... Ability to deliver software through the entire product development lifecyle, ensuring smooth and ...

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 ... product development lifecyle, ensuring smooth and efficient operations from initial planning ...

Bdx

BD Engineering Development Program

Durham, NC

... medical device instrumentation and applications. A successful candidate will work under the supervision of an R&D manager and team to develop and maintain medical technology and devices. They work to ...

Arclin

Product Development Chemist

Moncure, NC · On-site

Reporting to the Product Development and Applications Manager , this position is responsible for designing and executing tasks associated with the development of innovative chemistry-based products ...

Arclin USA LLC

Product Development Chemist

Moncure, NC · On-site

Reporting to the Product Development and Applications Manager , this position is responsible for designing and executing tasks associated with the development of innovative chemistry-based products ...

Arclin

Product Development Chemist

Moncure, NC · On-site

Reporting to the Product Development and Applications Manager , this position is responsible for designing and executing tasks associated with the development of innovative chemistry-based products ...

Senzit

Business Development Manager

Raleigh, NC · On-site

Collaborate closely with cross-functional teams, including marketing, product development, and ... Proven experience as a Business Development Manager in the heavy-duty equipment and off-road diesel ...

Senzit

Business Development Manager

Raleigh, NC · On-site

Collaborate closely with cross-functional teams, including marketing, product development, and ... Proven experience as a Business Development Manager in the heavy-duty equipment and off-road diesel ...

Fulfill Team Inc.

Be Seen First

C# Developer / Engineer

Raleigh, NC · On-site

$100K - $130K/yr

IEC 62304 - - Medical Device Software Standard - willing to learn * ISO 13485 - preferred * ISO ... product development. * Completes assigned training and development courses assigned by management ...

Trilliant Networks

Product Manager

Cary, NC · On-site

$90 - $130/hr

We are a device-agnostic, integrated, multi-technology communication platform that provides ... Manage the full product lifecycle -- from concept and development through general availability to ...

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All JobsMedical Device Product Development JobsMedical Device Product Development Manager JobsMedical Device Product Development Manager Jobs in Raleigh, NC

Medical Device Product Development Manager information

See Raleigh, NC salary details

$41.3K

$123.4K

$140.5K

How much do medical device product development manager jobs pay per year?

As of Sep 5, 2026, the average yearly pay for medical device product development manager in Raleigh, NC is $123,442.00, according to ZipRecruiter salary data. Most workers in this role earn between $111,300.00 and $139,000.00 per year, depending on experience, location, and employer.

What does a medical device product development manager do?

A Medical Device Product Development Manager oversees the entire process of bringing a medical device from the concept stage to market launch. They coordinate cross-functional teams, manage timelines, ensure compliance with regulatory standards, and oversee testing and validation of products. Their responsibilities also include working with engineers, designers, and regulatory specialists to ensure the device meets safety, efficacy, and user needs. Ultimately, they play a critical role in ensuring that new medical devices are developed efficiently, safely, and in compliance with industry standards.

How does a medical device product development manager typically collaborate with cross-functional teams during the development process?

A Medical Device Product Development Manager works closely with cross-functional teams, including engineering, regulatory affairs, quality assurance, marketing, and clinical experts, to ensure that product requirements are met throughout each development phase. They facilitate regular meetings to align on project milestones, address potential risks, and incorporate feedback from various stakeholders. This collaborative environment helps ensure that the final product complies with regulatory standards and meets market needs, making strong communication and project management skills essential in this role.

What are the key skills and qualifications needed to thrive as a medical device product development manager, and why are they important?

To thrive as a Medical Device Product Development Manager, you need expertise in engineering or life sciences, experience with product lifecycle management, and knowledge of regulatory requirements, often supported by a relevant degree. Familiarity with CAD software, project management tools, and compliance systems such as ISO 13485 or FDA regulations is typically required. Strong leadership, cross-functional communication, and problem-solving skills help drive innovation and align diverse teams. These competencies are vital to ensure products are developed efficiently, safely, and in compliance with industry standards.

What is the difference between Medical Device Product Development Manager vs Medical Device Quality Assurance Specialist?

AspectMedical Device Product Development ManagerMedical Device Quality Assurance Specialist
CredentialsEngineering degree, certifications like PMP or PDMAQuality assurance certifications like CQE, ISO auditor
Work EnvironmentDesign teams, R&D, cross-functional project groupsQuality labs, compliance departments, manufacturing oversight
Industry UsageLeading product development from concept to launchEnsuring products meet quality and regulatory standards

The Medical Device Product Development Manager focuses on designing and developing new medical devices, managing cross-functional teams, and bringing products to market. In contrast, the Medical Device Quality Assurance Specialist ensures that products meet quality standards and regulatory requirements throughout the development and manufacturing process. Both roles are essential in the medical device industry but serve different functions in product lifecycle management.

What is medical device product development?

Medical device product development involves designing, testing, and bringing new medical devices to market, ensuring they meet safety and regulatory standards. A Medical Device Product Development Manager oversees this process, coordinating cross-functional teams, managing timelines, and ensuring compliance with industry regulations such as FDA or ISO standards.
Medical Device Product Development Manager jobs near you
Infographic showing various Medical Device Product Development Manager 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 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $123,442 per year, or $59.3 per hour.

Sr. Engineer, Software Dev, R&D

Teleflex

Morrisville, NC • On-site

$114K - $151K/yr

Full-time

Posted 19 days ago

Teleflex rating

8.3

Company rating: 8.3 out of 10

Based on 27 frontline employees who took The Breakroom Quiz

Job description

Expected Travel: Up to 10%
Requisition ID: 14269

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, Rusch, 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 Senior Engineer specializing in Software, you will advance technological innovations in vascular positioning systems, including artificial intelligence/machine learning (AI/ML), application software, and embedded software systems. 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 achieve reliable and predictable software releases.

Principal Responsibilities

   Lead the development of software for connected medical device software systems, ensuring scalability, reliability, and maintainability.
   Design and develop medical device software that is high quality, safe, secure and compliant.
   Lead software developers, third-party designers, vendors, and contractors to deliver high-quality software solutions. 
   Own software design control activities and documentation efforts, including software development planning, software requirements, software risk mitigations, software detailed design, traceability, software reviews, and software releases.
   Ability to deliver software through the entire product development lifecyle, ensuring smooth and efficient operations from initial planning through development, testing, deployment of software features, and software maintenance
   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 Engineering, Electrical Engineering or equivalent with appropriate experience.
   6+ years of software development in senior development, preferably with lead role experience, preferably in medical devices or regulated industry, with a proven track record of deployment in commercial products.

Specialized Skills / Other Requirements

   Experience and depth of understanding of modern programming languages (C++ and C#) and design patterns utilized within embedded systems applications.

   Experience developing medical device software within an embedded operating system (such as Linux).
   Experience in creating software solutions 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).
   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. 
   Ability to solve problems for end users, with an ability to translate into software requirements, design, and test specifications. 
   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).
   Familiarity with Electronic Medical Record (EMR) 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. 

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, Rusch, 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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