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Junior Medical Device Software Engineer Jobs (NOW HIRING)

Sr. Engineer, Software Dev, R&D

Morrisville, NC · On-site

$114K - $151K/yr

... Engineer specializing in Software, you will advance technological innovations in vascular ... Principal Responsibilities • Lead the development of software for connected medical device ...

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 software developers, third-party designers, vendors, and contractors to deliver high-quality software ...

Support compliance considerations related to regulated medical device software development practices. * Document findings and recommendations to facilitate efficient handoff to permanent engineering ...

Principal, Software Engineer

Lake Forest, CA · On-site

$143K - $192K/yr

The Principal Software Engineer, Medical Device Systems is responsible for maintaining, enhancing, and supporting software for Alcon's on-market ophthalmic medical devices and imaging platforms. This ...

Review quality system documentation products as they apply to the development, verification, validation, use, and maintenance of medical device software. Coordinate activities with other engineering ...

... Engineer will own software design control strategy, processes, documentation, and continuous ... Own software design control impact assessments for design changes within the medical device design ...

Showing results 41-60

Junior Medical Device Software Engineer information

See salary details

$46.5K

$94.5K

$142K

How much do junior medical device software engineer jobs pay per year?

As of Sep 4, 2026, the average yearly pay for junior medical device software engineer in the United States is $94,542.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,000.00 and $95,500.00 per year, depending on experience, location, and employer.

What does a junior medical device software engineer do?

A Junior Medical Device Software Engineer assists in designing, developing, testing, and maintaining software for medical devices under the supervision of senior engineers. They help ensure that the software meets regulatory standards for safety and performance. Their work may involve writing code, debugging, documenting processes, and collaborating with cross-functional teams such as hardware engineers and quality assurance. This role is ideal for recent graduates or those with a few years of experience looking to build a career in the intersection of healthcare and technology.

What are the key skills and qualifications needed to thrive as a junior medical device software engineer?

To thrive as a Junior Medical Device Software Engineer, you need a solid background in software development (often with a degree in computer science or biomedical engineering), knowledge of medical device regulations, and familiarity with embedded systems. Experience with programming languages like C/C++, development environments, and compliance with standards such as IEC 62304 are typically required. Attention to detail, problem-solving abilities, and strong teamwork and communication skills help you excel in this role. These competencies are essential to ensure the safe, effective, and compliant development of medical device software in a highly regulated industry.

What are some common challenges faced by junior medical device software engineers in their first year on the job?

Junior Medical Device Software Engineers often encounter challenges such as adapting to strict regulatory standards, learning thorough documentation practices, and understanding the complexities of safety-critical software development. Working in multidisciplinary teams, they must quickly become proficient in both software engineering and medical device compliance, such as FDA or ISO standards. Successfully navigating these challenges requires strong communication skills, attention to detail, and a willingness to learn from senior engineers and cross-functional colleagues.

What is the difference between Junior Medical Device Software Engineer vs Medical Device Software Engineer?

AspectJunior Medical Device Software EngineerMedical Device Software Engineer
Required CredentialsTypically an entry-level degree (BSc or MSc) in Software Engineering, Biomedical Engineering, or related fields; may include basic certificationsSame as junior, but often with more professional experience or advanced certifications
Work EnvironmentSupportive team settings within medical device companies or healthcare tech firmsMore independent roles with increased responsibility in design, testing, and validation
Employer & Industry UsageCommonly used in medical device manufacturing, healthcare technology companies, and startupsUsed across medical device companies, regulatory bodies, and R&D departments

The main difference between a Junior Medical Device Software Engineer and a Medical Device Software Engineer lies in experience and responsibility. Junior roles focus on learning and supporting development tasks, while the more experienced engineer takes on complex design and validation responsibilities.

What cities are hiring for Junior Medical Device Software Engineer jobs?

Cities with the most Junior Medical Device Software Engineer job openings:

What are the most commonly searched types of Medical Device Software Engineer jobs?

The most popular types of Medical Device Software Engineer jobs are:

What states have the most Junior Medical Device Software Engineer jobs?

States with the most job openings for Junior Medical Device Software Engineer jobs include:

Infographic showing various Junior Medical Device Software Engineer job openings in the United States as of July 2026, with employment types broken down into 77% Full Time, 14% Part Time, and 9% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $94,542 per year, or $45.5 per hour.

Sr. Engineer, Software Dev, R&D

Teleflex

Morrisville, NC • On-site

$114K - $151K/yr

Full-time

Posted 18 days ago


Key responsibilities

  • Lead the development of software for connected medical device systems, ensuring scalability, reliability, and maintainability.

  • Design and develop high-quality, safe, secure, and compliant medical device software.

  • Own software design control activities, including planning, requirements, risk mitigation, detailed design, reviews, and releases.


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™, 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 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™, 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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