Medical Device Development Internship in Houston, Texas
Medical Device Development Internship in Houston, Texas
- April 5, 2023
- Posted by: Interns

- Internship
- San Francisco, California

Internships USA
Marketing Content Creator Internship
Position: Medical Device Development Internship
Location: Houston, Texas
Language: English
Duration: 6-24 months
Compensation: to be discussed
Job description
Our partner is seeking a Medical Device Development Intern to join their team for a 10 moths internship. The intern will support the research and development of medical devices within a healthcare organization in Houston, Texas. The intern will work closely with the Senior Medical Device Engineer and other members of the R&D team to design, test, and refine medical devices, with the goal of improving patient outcomes and advancing the field of healthcare technology.
Responsibilities:
- Assist in the design and development of medical devices, including concept ideation, CAD modeling, prototyping, and testing.
- Collaborate with cross-functional teams, including clinicians, engineers, and regulatory specialists, to ensure that medical devices meet clinical and regulatory requirements.
- Conduct literature reviews and market analyses to identify unmet clinical needs and opportunities for innovation in the medical device field.
- Participate in user testing and feedback sessions to gather input on device usability, performance, and safety.
- Document design and testing activities in technical reports, presentations, and other formats as needed.
- Stay up-to-date with emerging technologies, regulatory requirements, and industry best practices in medical device development.
Profile
Education: Currently enrolled in a Bachelor’s or Master’s degree program in biomedical engineering, mechanical engineering, electrical engineering, or a related field. Recent graduates may also be considered.
Competences and qualifications
- Strong academic record with coursework in medical device design, biomechanics, materials science, and/or regulatory affairs.
- Experience with CAD software, such as SolidWorks, and rapid prototyping tools, such as 3D printers and CNC machines.
- Familiarity with medical device regulations, such as FDA 510(k) and ISO 13485.
- Excellent communication, teamwork, and problem-solving skills.
- Self-starter with a strong work ethic and a desire to learn and contribute to a dynamic team.
A unique opportunity awaits! Make your move now – reach out today for more details or any other questions you may have.
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