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Internship R&D Engineer Medical Device Jobs in Massachusetts

BEPC INC

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Medical Device Assembler

Westford, MA · On-site

$19 - $21.50/hr

Medical Device Assembler Location : Westford, MA Employment Type : Full-Time| 6 Month contract | W2 ... technology, engineering, manufacturing, and project management. At BEPC , we are driven by ...

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Internship R D Engineer Medical Device information

What does an internship R&D engineer 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 types of projects or tasks can an internship R&D engineer medical device expect to work on?

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 are the key skills and qualifications needed to thrive as an internship R&D engineer medical device?

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 cities in Massachusetts are hiring for Internship R&D Engineer Medical Device jobs?

Cities in Massachusetts with the most Internship R&D Engineer Medical Device job openings:

Internship R D Engineer Medical Device jobs near you

Medical Device Test Engineer

Conflux Systems

Newton, MA • On-site

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

We are seeking a Contract System Test Engineer to support verification activities for a complex medical robotics system used in advanced robotic-assisted vascular interventions. The role focuses on developing and executing system-level testing, ensuring product requirements traceability, and supporting verification and validation for complex electromechanical medical devices. The ideal candidate will contribute to quality processes, implement verification methods, and support continuous improvement across systems engineering and testing workflows.
Responsibilities:
  • Develop and implement test methods for verification of complex medical robotic systems.
  • Execute system and subsystem verification testing during verification and validation (V&V) phases.
  • Maintain and update requirements traceability and risk management documentation.
  • Implement processes within verification and issue management toolchains.
  • Perform statistical analysis and determine sample size for tests using statistical methods.
  • Validate software tools and test fixtures used in testing activities.
  • Support continuous improvement of systems engineering and quality processes.

Qualifications:
  • Bachelor's degree in Systems Engineering, Biomedical Engineering, Robotics, Software Engineering, Mechanical Engineering, or Electrical Engineering.
  • 5+ years of experience in medical device testing, preferably with medical or surgical robotics systems.
  • Strong knowledge of verification strategy development, test method validation, and requirements traceability.
  • Experience with IEC 60601-1 and related medical device standards.
  • Background in electromechanical systems testing, statistical test analysis, and verification toolchain implementation.
  • Experience supporting complex medical device programs through verification and validation phases.

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