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Internship R&D Engineer Medical Device Jobs in Houston, TX

A.A.D Co.

Medical Device Account Manager

Houston, TX · On-site

Residency within forty miles of the advertised location * 3 Years Prior Medical Imaging (RT(R)) or Medical Equipment/Device Sales experience * Willing to travel daily, sometimes overnight * Astable ...

Danaher

Software Engineer Internships

The Woodlands, TX · On-site

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 ...

Danaher

Software Engineer Internships

Houston, TX · On-site

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 ...

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Internship R D Engineer Medical Device information

See Houston, TX salary details

$10

$18

$28

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

As of Aug 21, 2026, the average hourly pay for internship r&d engineer medical device in Houston, TX is $18.44, according to ZipRecruiter salary data. Most workers in this role earn between $15.38 and $19.95 per hour, depending on experience, location, and employer.

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 near Houston, TX are hiring for Internship R&D Engineer Medical Device jobs?

Cities near Houston, TX with the most Internship R&D Engineer Medical Device job openings:

Internship R D Engineer Medical Device jobs near you

Client & Scientific Solutions Intern

Medical Metrics

Houston, TX • On-site

$13.75 - $18.25/hr

Full-time, Internship

Posted 11 days ago

Job description

COMPANY & COMPENSATION:
• Medical Metrics Inc. (MMI) is a fast-growing, independent imaging core laboratory based in Houston, TX. MMI provides image analysis and consulting services to medical device, biologics, and pharmaceutical companies in support of their clinical trials and product R&D.
• Competitive hourly rate, commensurate with academic standing and qualifications
• Structured mentorship, exposure to multiple CSS functions, and consideration for full-time positions such as Client Services Associate upon graduation
JOB SUMMARY:
Medical Metrics, Inc. (MMI) is seeking a Client & Scientific Solutions (CSS) Intern to join its Houston, TX team for a paid, three-month internship. CSS is responsible for the scientific and client-facing aspects of MMI's imaging services offerings. The intern will work alongside imaging scientists, biomedical engineers, analysts, and client services professionals in support of the clinical trials business for medical device, biologics, and pharmaceutical companies.
The internship is designed as a broad, mentored introduction to the field of imaging where it intersects with clinical research and product development. Interns receive training in how quantitative imaging data is generated and reviewed, contribute to the scientific and technical content of client proposals and study documents, and conduct scientific literature and market research that informs study design and business strategy. Assignments are shaped around each intern's technical strengths and career interests, with the goal of building practical skills that are transferrable to a roles in image analysis, scientific consulting, and client engagement.
DUTIES AND RESPONSIBILITIES MAY INCLUDE:
Data & Analytics (DA) support
  • Conduct image analysis under the supervision and guidance of experienced engineers, analysts, and scientists, following the applicable Standard Operating Procedures (SOPs) and work instructions
  • Learn how imaging data is evaluated for quality and protocol conformance, and contribute observations to the team review process
  • Contribute to quality assurance/control checks, data reconciliation, and preparation of analysis datasets
  • Assist the team in compiling summary statistics, tables, and figures from analysis output

Client Services (CS) support
  • Contribute to proposal development as part of the CS team, including drafting sections of scope of work narratives and assembling proposal documents for clinical trials
  • Participate in the preparation of capabilities presentations, RFI and RFP responses, and client-facing collateral
  • Conduct competitive, market, and therapeutic area research, contributing findings that inform proposal and business development activity
  • Participate in preparations for investigator and coordinator meetings, tradeshows, and workshops

Consulting support
  • Contribute to the development of imaging protocols under the direction of scientific staff
  • Compile and summarize relevant scientific literature, society guidelines, and regulatory guidance in support of the team's study design recommendations
  • Assist in the preparation of consulting deliverables such as endpoint recommendations and technical memos
  • Participate in the review of sponsor documents, including clinical protocols and statistical analysis plans, for imaging-related content, noting questions for discussion

General
  • Maintain accurate, well-organized documentation of all work performed
  • Communicate progress, questions, and obstacles promptly to the internship supervisor
  • Complete an end-of-term project summary and present it to the CSS team
  • Understand MMI's Quality Policy, support the achievement of the organization's quality objectives, and escalate issues that present organizational risk
  • Comply with company policies and procedures, as well as ISO 9001 and Current Good Clinical Practices (cGCPs) related to job tasks

Requirements
EDUCATION AND EXPERIENCE:
  • BS in Bioengineering, Biomedical Engineering, or a related discipline; candidates in the final semester of a BS program may also be considered
  • Coursework or project experience in medical imaging, image processing, biomechanics, anatomy, or physiology preferred
  • Prior research, co-op, or laboratory experience is preferred

SKILLS REQUIRED:
  • Exceptional attention to detail and follow-through
  • Excellent written and verbal communication skills
  • Strong analytic, quantitative, and computer skills
  • Ability to follow written procedures precisely and to document work clearly
  • Ability to rapidly acquire and apply new technical and scientific knowledge
  • Ability to compile, synthesize, and interpret relevant scientific literature
  • Ability to manage multiple assignments under defined timelines with appropriate supervision
  • Highly self-motivated, with the judgment to ask questions and seek guidance when needed
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook)

PLUSES:
  • Familiarity with diagnostic imaging and radiology (e.g., XR, CT, MRI, Ultrasound)
  • Hands-on experience with image analysis or segmentation software (e.g., ImageJ, 3D Slicer)
  • Coursework or research related to anatomy and/or imaging of spine, musculoskeletal system cardiovascular system, CNS, and/or ENT
  • Understanding of clinical trials, including the US-FDA 510(k) / PMA regulatory pathways
  • Technical writing experience

Apply