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

Medical Device Engineer I

Rochester, NY · On-site

$65K - $100K/yr

The Medical Device Engineer II supports the design and development of contact lenses within Bausch + Lomb's Vision Care R&D organization. This role serves as a product advocate on cross-functional ...

By submitting your interest, you'll be among the first to know when internship opportunities open ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...

By submitting your interest, you'll be among the first to know when internship opportunities open ... Producing documentation to support medical device regulatory processes Who This Is For * Students ...

Set your own hours and tutor as much as you'd like. * Tutor remotely using our purpose-built Live ... Skilled at breaking down physiological system modeling, biomechanical analysis, and medical device ...

Senior DevOps Engineer

Rochester, NY · Remote

$128K - $164K/yr

This role will focus on the design, implementation, and operation of Azure DevOps-centric CI/CD pipelines that support safetycritical, regulated medical device software. The DevOps Engineer will ...

Lead Metrology Engineer

West Henrietta, NY · On-site

$98K - $129K/yr

... R&D. This position combines deep expertise in optical metrology with hands-on system design and ... The engineer will drive innovation in measurement science, execute technical direction, and enable ...

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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 30, 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:
Infographic showing various Internship R&D Engineer Medical Device job openings in Rochester, NY as of June 2026, with employment types broken down into 86% Full Time, and 14% Contract. Highlights an 100% In-person job distribution, with an average salary of $39,639 per year, or $19.1 per hour.
Validation Engineer (Medical Device)

Validation Engineer (Medical Device)

Caresoft

Rochester, NY • On-site

Other

Posted 17 days ago


Job description

Title: Valdiation Engineer (Medical Device)
Location: Rochester NY

Duration: 12 Months

Overview:
This role supports validation activities for new products within a medical device manufacturing facility and requires the ability to work both independently and as part of a cross-functional team.
Key Responsibilities
Support validation work for new products, including laboratory testing utilizing VITROS analyzers.
Prepare and handle clinical test specimens according to approved procedures, best practices, and safety requirements, including appropriate PPE.
Perform pilot-scale formulations with biological materials, as needed.
Operate and maintain laboratory equipment; complete all required documentation in real time (QC records, instrument logs, test records).
Independently execute laboratory experiments and assist with troubleshooting instrument and test failures, as needed.
Review and analyze data; document conclusions and test summaries in appropriate quality records within QuidelOrtho's quality system.
Ensure organization, documentation, and tracking of long-term studies with multiple factors, products, and conditions.
Maintain a working knowledge of cGMP requirements and adhere to all quality, regulatory, and safety guidelines.
This role involves both laboratory and computer-based work.
Skills Required:
Bachelor's degree in a scientific field (e.g., Chemistry, Biology, or equivalent) required.
Experience in an FDA-regulated industry and in validation for medical devices preferred.
Familiarity with VITROS products and VITROS analyzers highly desired.
Familiarity with biological formulations and processing techniques highly desired.
Strong written and verbal communication skills with excellent attention to detail required.
Strong organizational skills and ability to manage complex, long-term studies required.
Proficiency in Excel required, with additional statistical analysis skills preferred.