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

Bausch + Lomb

Compliance Engineer II

Rochester, NY · On-site

$65K - $100K/yr

The Compliance Engineer II will provide technical support of Departmental Technical Documentation ... ISO-9000, GMP, medical device manufacturing experience, technical writing, equipment and software ...

IDEX Corporation

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 ...

Kodak

Regulatory Affairs Lead

Rochester, NY

$125K - $130K/yr

Bachelor's degree in Life Sciences, Biomedical Engineering, Regulatory Affairs, or a related field required. 6-8 years of Regulatory Affairs experience within the medical device industry.

Kodak

Regulatory Affairs Lead

Rochester, NY · On-site

$125K - $130K/yr

... Engineering, Regulatory Affairs, or a related field required. • 6-8 years of Regulatory Affairs experience within the medical device industry. • Demonstrated hands-on experience preparing and ...

onsemi

Yield and Device Engineering Manager

Hopewell, NY · On-site

$127K - $217K/yr

The Yield, Device, and Integration Engineering Manager leads a multidisciplinary organization of ... medical condition, genetic information, military or veteran status, gender identity, gender ...

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Internship R D Engineer Medical Device information

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$10

$19

$29

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

As of Jul 22, 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:
Internship R D Engineer Medical Device jobs near you
Infographic showing various Internship R&D Engineer Medical Device job openings in Rochester, NY as of July 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.
Compliance Engineer II

Compliance Engineer II

Bausch + Lomb

Rochester, NY • On-site

$65K - $100K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted yesterday

Bausch & Lomb rating

8.6

Company rating: 8.6 out of 10

Based on 39 frontline employees who took The Breakroom Quiz

26th of 534 rated manufacturers

Job description

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world-from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better.
Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future.
The Compliance Engineer II will provide technical support of Departmental Technical Documentation activities and the development, implementation and effectiveness of Development Process Engineering's (DPE's) procedures and systems for compliance to the quality directives. This includes but is not limited to gap assessments of directives and DPE's processes and procedures, training, procedure effectiveness, metrics for tracking performance, qualification and validation support of equipment, facilities and software, conducting risk assessments, technical writing and electronic filing and storage of information, support internal audits and corrective actions.
Responsibilities:
  • Support Process Engineering Lab Quality Directives gap analysis and closure plan execution.
  • Perform risk assessments, investigations, documentation and procedure updates, qualification writing and execution.
  • Drive effort to manage DPE's SOPs to ensure GMP, FDA, and ISO compliance.
  • Support Compliance and Documentation Systems for DPE (Global Document Management System for protocols/reports and procedures; CATSWeb for non-conformances and CAPAs; Compliance Wire Learning
  • Management System for training; Kintana for change control, conduct risk assessments as they pertain to Quality System compliance.
  • Support systems for PMs, Calibration, Environmental Monitoring, and storage of clinical trial materials and products.
  • Manage and maintain the Master Validation plan for the qualification and requalification of equipment, facilities and software.

Requirements:
  • Bachelors Degree in Science/Engineering strongly preferred and/or certification as a Quality Engineer.
  • 3+ years' experience with medical devices and/or clean room environment compliance regulations with Quality Engineering experience strongly desired
  • Specialized Training: ISO-9000, GMP, medical device manufacturing experience, technical writing, equipment and software qualification documentation, Lean/Six sigma
  • Special Skills: Computer competent with Microsoft Office suite; ability to learn specific software systems utilized in B&L's growing Quality Systems (Documentum, Kintana, CATSWeb).
  • Ability to develop working relationships with various internal core competencies and work as a team member.
  • Active participation in Process and Design FMEA activities
  • Strong Communication, Organization, Report Writing skills

Preferences:
  • Regulated Medical Device or Pharma industry
  • Use and knowledge of Lean and DFSS tools and software

We offer competitive salary & excellent benefits including:
• Medical, Dental, Eye Health, Disability and Life Insurance begins on your hire date
• 401K Plan with company match and ongoing company contribution
• Paid time off - vacation (3 weeks - prorated upon hire), floating holidays and sick time
• Employee Stock Purchase Plan with company match
• Employee Incentive Bonus
• Tuition Reimbursement (select degrees)
• Ongoing performance feedback and annual compensation review
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
For U.S. locations that require disclosure of compensation, the starting pay for this role is between $65,000.00 and $100,000.00. The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors.
U.S. based employees may be eligible for short-term and/or long-term incentives. They may also be eligible to participate in medical, dental, vision insurance, disability and life insurance, a 401(k) plan and company match, a tuition reimbursement program (select degrees), company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive sick time, floating holidays and paid vacation.
Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms.
To learn more please read Bausch + Lomb's Job Offer Fraud Statement.
Our Benefit Programs: Employee Benefits: Bausch + Lomb
Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

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About Bausch & Lomb

Sourced by ZipRecruiter

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world--from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better. Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our nearly 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 12,500 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Bridgewater, NJ, US

Year founded

1853

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