Name: Ananya Eashwer
Major and College: Master’s student in Biomedical/ Medical Engineering at The Johns Hopkins University
Internship Title: Quality and Regulatory Affairs Intern
Internship Site: Infinite Biomedical Technologies
1) Please tell us about your career goals.
My career goal is to become a medical device engineer focused on developing innovative, patient-centered technologies that improve quality of life! I am particularly interested in working across the full product lifecycle, from concept and design to verification, regulatory approval, and manufacturing. Through my experience at IBT, I have developed a strong interest in prosthetics and rehabilitation devices, and I hope to continue contributing to technologies that restore function and independence for patients. Long-term, I want to take on leadership roles where I can drive impactful product development while ensuring safety, quality, and regulatory compliance.
2) Tell us about your internship (i.e., day-to-day responsibilities, special projects/clients, and work culture).
During my internship, I support regulatory and quality activities to ensure compliance with FDA and ISO standards. I assist with supplier qualification by coordinating with vendors and gathering required documentation, perform incoming inspection of components, and help complete change orders and regulatory documentation. I also support production and testing, gaining hands-on experience with device assembly and quality checks. The role is highly collaborative, working closely with engineering, manufacturing, and quality teams to ensure safe and effective products.
3) Describe the process of obtaining your position. When did you hear of the position and submit your application?
I applied for this role through Handshake, went through the interview process, and have continued working here since joining the team.
4) Which of the following resources did you use to find your current experience?
MTIP Website, Handshake or other job boards, Career Fairs, Faculty Connections
5) What have you enjoyed the most about your position or organization?
I’ve most enjoyed the opportunity to work across regulatory, quality, and production, which has given me a holistic view of the medical device lifecycle. I also value the collaborative environment and the ability to contribute to products that directly impact patients.
6) How do you believe you have made an impact through your work?
I’ve contributed by supporting regulatory and quality processes that ensure devices are safe and compliant. Through supplier qualification, incoming inspection, and documentation support, I’ve helped maintain product quality and streamline operations across teams.
7) What advice would you give to another student who is seeking an internship or similar experience (i.e., Internship search, Resume, or Interview tips)?
Don’t hesitate to reach out, ask questions, and connect with others. Networking and tailoring your resume to each role can go a long way in securing opportunities.