1

Internship R&D Engineer Medical Device Jobs in Rochester, NY

A., D.P.C. has created an internship program to engage college students that are ready to get their ... device, or medical service), marital status, partnership status, caregiver status, domestic ...

CNC Lead SetUp

Rochester, NY · On-site

$80K - $100K/yr

The engineer will serve as a technical expert, mentor, and key contributor to continuous ... Experience in high-precision or regulated industries such as aerospace, medical device, or ...

The engineer will serve as a technical expert, mentor, and key contributor to continuous ... Experience in high-precision or regulated industries such as aerospace, medical device, or ...

... medical device phase gate process resulting in approvals or working in a regulated environment (e.g. FDA, ISO, etc.). * Bachelor's degree in engineering, Life Sciences, Business, or related field.

Senior Software Engineer

Rochester, NY

$120K - $159K/yr

... a medical device environment or equivalent combination of education and experience. * Experience ... Systems Engineers, Hardware Engineers, Quality/Regulatory, Operations, Marketing, Manufacturing ...

Senior Software Engineer

Rochester, NY

$120K - $159K/yr

... a medical device environment or equivalent combination of education and experience. * Experience ... Systems Engineers, Hardware Engineers, Quality/Regulatory, Operations, Marketing, Manufacturing ...

next page

Showing results 1-20

Internship R D Engineer Medical Device information

See Rochester, NY salary details

$10

$19

$29

How much do internship r&d engineer medical device jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for internship r&d engineer medical device in Rochester, NY is $19.06, according to ZipRecruiter salary data. Most workers in this role earn between $15.91 and $20.62 per hour, depending on experience, location, and employer.

What does an Internship R&D Engineer in Medical Device do?

An Internship R&D Engineer in Medical Device assists in the research and development of new medical technologies and products. Their responsibilities typically include supporting senior engineers in designing, testing, and improving medical devices, conducting experiments, collecting and analyzing data, and preparing technical documentation. Interns also learn about regulatory standards and industry best practices while working as part of a multidisciplinary team. This role is ideal for students or recent graduates looking to gain hands-on experience in medical device innovation.

What are the key skills and qualifications needed to thrive as an Internship R&D Engineer in Medical Devices, and why are they important?

To thrive as an Internship R&D Engineer in Medical Devices, you generally need a background in biomedical engineering or a related field, with strong analytical and problem-solving abilities. Familiarity with CAD software, lab equipment, and basic knowledge of regulatory standards like ISO 13485 is important, and prior internships or relevant coursework can be advantageous. Attention to detail, effective communication, and collaborative teamwork skills help you contribute meaningfully to projects and navigate cross-functional environments. These skills ensure you can support innovative product development while adhering to strict safety and quality standards in the medical device industry.

What is the difference between Internship R&D Engineer Medical Device vs R&D Engineer Medical Device?

AspectInternship R&D Engineer Medical DeviceR&D Engineer Medical Device
QualificationsEnrolled in or recent graduate of engineering/biomedical programsBachelor's or Master's in engineering/biomedical fields
Work EnvironmentInternship programs, entry-level projects, supervised tasksFull-time, independent project work, team collaboration
ResponsibilitiesAssisting in research, testing, and documentationDesign, develop, and improve medical device products
Industry UsageCommonly used for training and entry-level experienceCore role in product development and innovation

In summary, the Internship R&D Engineer Medical Device is an entry-level position designed for students or recent graduates gaining initial industry experience. The R&D Engineer Medical Device is a full-time professional role with greater responsibilities in product development and innovation within the medical device industry.

What types of projects or tasks can an Internship R&D Engineer expect to work on in the medical device industry?

As an Internship R&D Engineer in the medical device industry, you can expect to be involved in a variety of projects such as prototyping new device concepts, conducting laboratory experiments, performing data analysis, and supporting design verification and validation activities. Interns often collaborate closely with multidisciplinary teams, including senior engineers, regulatory specialists, and clinicians, to help solve real-world problems and improve patient outcomes. This hands-on experience provides valuable insight into the product development lifecycle and offers opportunities to contribute to meaningful projects that can enhance your technical and professional skills.
What cities near Rochester, NY are hiring for Internship R&D Engineer Medical Device jobs? Cities near Rochester, NY with the most Internship R&D Engineer Medical Device job openings:
Lead Systems Integration Engineer

Lead Systems Integration Engineer

Carestream Health

Rochester, NY • On-site

$155K - $175K/yr

Full-time

Posted 4 days ago


Job description

Innovation that sparks imagination. Continue on to your next challenge with us.
Carestream is a worldwide provider of medical imaging systems and solutions; x-ray imaging systems for non-destructive testing; manufacturing of film and precision contract coating services for a wide range of industrial, medical, electronic and other applications-all backed by a global service and support network. Carestream's diagnostic imaging technology systems are at work in 90 percent of hospitals worldwide.
At Carestream, we offer a global perspective and a world of opportunities for people who have the desire to make a positive impact. Join our global team!
Relocation stipend available
Compensation: $155,000 - $175,000 per year
*This range reflects Carestream's good faith estimate to pay fairly as starting wage. Offers will be tailored within the range based on the selected candidate's experience, industry knowledge, technical and communication skills, and other factors that may prove relevant during the interview process, as well as geographic market differentials for the position.
Position Summary:
The Lead Systems Integration Engineer serves as the technical and commercial bridge between market needs, product strategy, and engineering execution across business segments. This role combines deep expertise in systems, automation, and product engineering to shape market aligned solutions, influence product direction, and support go to market strategies within the product portfolios. They will lead solution definition, proof of concept activities, internal enablement, and executive level technical value discussions aligned with business objectives.
The position provides technical and architectural leadership for the design, development, and integration of complex medical imaging systems. It owns end to end system definition across hardware, software, firmware, and data domains, ensuring performance, reliability, regulatory compliance, and alignment with clinical and business goals.
The Lead Systems Integration Engineer partners closely with Platform Engineering, Product Management, Clinical, and Research Innovation teams to deliver scalable and differentiated medical imaging systems. The role is solution oriented and business informed, while remaining grounded in system integration and execution realities.
Position Responsibilities:
Systems Design and Architecture
• Defines and governs scalable system architectures integrating hardware, software, firmware, automation, data components, workflows, imaging pipelines, interfaces, and infrastructure into cohesive, high-performance, market-ready systems
• Leads integration strategies across hardware, software, firmware, and data into unified imaging platforms
• Applies Model-Based Systems Engineering (MBSE) to capture requirements, system behavior, interfaces, and constraints with full traceability
• Translate clinical, business, and regulatory needs into clear system requirements and architectural solutions
• Ensures alignment with platform and portfolio strategy while enabling configuration, reuse, and scalability
• Evaluates architecture options and build-versus-buy decisions, balancing technical, financial, operational, and risk considerations
• Leads design reviews, facilitates technical discussions, and drives trade studies to optimize performance, reliability, cost, and scalability
• Collaborate with cross-functional teams and external partners to align architecture with portfolio and segment goals
• Drives modeling, simulation, and prototyping to validate architecture and reduce integration risk early in development
• Establishes best practices for solution definition, technical communication, and market alignment
Required Skills & Education:
Education
• Bachelor's or Master's degree in Systems Engineering, Mechatronics Engineering, Computer Engineering, Robotics Engineering, Automation Engineering, Electrical Engineering, Biomedical Engineering or a related STEM field
Experience
• 7+ years in systems architecture, systems integration, or complex product development in medical imaging, medical devices, or other regulated industries
Skills
• Strong foundation in systems engineering practices, including MBSE and requirements management
• Experience with hardware/software integration, system modeling, Hardware-in-the-loop (HIL) and Sim-to-Real test and prototyping
• Strong problem-solving, risk assessment, and technical decision-making skills
• Excellent communication skills, with the ability to break down and explain complex concepts to a diverse audience
Desired Skills:
Experience
• 10+ years in systems architecture or development within medical imaging or regulated medical device environments
• Past related work with sales engineering, applications engineering, solution architecture, and product focused engineering roles, supported by formal training in industrial, computer, or automation engineering
Skills
• Experience with regulated development frameworks (e.g., FDA 21 CFR Part 820, IEC 62304)
• Advanced experience with modeling tools, digital thread concepts, and system-level V&V strategies
Work Environment:
Office environment
Carestream is an Equal Opportunity Employer
Carestream is an equal opportunity organization. We recruit, employ, train, compensate, and promote without regard to race, religion, creed, color, national origin, age, gender, sexual orientation, gender identity, marital status, disability, veteran status, or any other basis protected by applicable federal, state or local law.
Applying for a job with Carestream
All applicants must complete the on-line application process. Carestream is committed to working with and providing reasonable accommodations to individuals with disabilities. If you require assistance or an accommodation because of a disability to participate in the application process, please click accommodations
Requisition ID: 4733