ZipRecruiter

Log In

1

Internship R&D Engineer Medical Device Jobs in Maryland

Inventwood

R & D Lab Technician

Frederick, MD · On-site

An associate's degree or technical certification in a science or engineering-technology field; a BS in Materials Science, Chemistry, Chemical or Mechanical Engineering, or a related field; or ...

New

Inventwood

R & D Project Manager

Frederick, MD · On-site

This is InventWood's first dedicated project management role in R&D. The team runs many concurrent ... A science or engineering background is a plus, not a requirement. * Fluent with modern project and ...

Inventwood

R & D Data Analyst

Frederick, MD · On-site

A BS in a quantitative or scientific field -- statistics, data science, engineering, physics, chemistry, materials science, or related -- and 3 - 5 years work experience in a related field. * Strong ...

next page

Showing results 1-20

All JobsR&D Engineer Medical Device JobsInternship R&D Engineer Medical Device JobsInternship R&D Engineer Medical Device Jobs in Maryland

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 Maryland are hiring for Internship R&D Engineer Medical Device jobs?

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

Internship R D Engineer Medical Device jobs near you

Senior Validation Engineer - Medical Devices

Stark Pharma Solutions Inc

Silver Spring, MD • On-site

Contractor

Re-posted yesterday

Job description

Job Title: Senior Validation Engineer – Medical Devices

Location: Silver Spring, MD (Onsite)

Duration: 06 months contract (High potential for extension)

Job Summary

We are seeking a Senior Validation Engineer to support equipment lifecycle management, facility changes, and commercialization activities within a medical device environment. This role will play a key part in ensuring equipment and systems are validated, compliant, and maintained in a validated state throughout their lifecycle.

The ideal candidate will have strong experience in validation documentation, equipment qualification, and cross-functional collaboration within regulated environments.

Key Responsibilities

Validation & Documentation

  • Develop, review, and execute validation documents including:
    • User Requirement Specifications (URS)
    • Validation Determination Assessments (VDA)
    • Installation, Operational, and Performance Qualifications (IQ/OQ/PQ)
    • Requirements Traceability Matrix (RTM)
    • Final/Summary Reports
  • Support equipment lifecycle validation activities for commercial medical device operations
  • Execute validation protocols and ensure compliance with regulatory standards

Required Qualifications

  • Minimum 5+ years of experience in validation within medical device or regulated environments
  • Strong experience with equipment lifecycle management and validation documentation
  • Hands-on experience with IQ/OQ/PQ, URS, RTM, and validation reporting
  • Experience supporting commercialization, facility changes, or system transitions
  • Knowledge of GMP, FDA, and quality system requirements
  • Strong collaboration, communication, and problem-solving skills