Joshita Majumdar
About Joshita Majumdar
Joshita Majumdar is a Product Innovation Manager at UE LifeSciences, where she leads the clinical validation and product development of medical devices. She has a background in biomedical engineering and has held various roles in research and project management across notable institutions, including Carnegie Mellon University and Apollo Hospitals.
Current Role at UE LifeSciences
Joshita Majumdar serves as the Product Innovation Manager at UE LifeSciences, a position she has held since 2018. Based in the Mumbai Area, India, she leads the clinical validation and product development of innovative medical devices, including iBreastExam Gen II and cervAIcal. Her responsibilities include transitioning these devices from concept to commercialization, ensuring they meet clinical and market needs.
Previous Experience at Tech Mahindra
Prior to her current role, Joshita worked at Tech Mahindra as a Business Manager for a duration of nine months in Bengaluru Area, India, from 2017 to 2018. In this position, she contributed to business operations and strategy, enhancing her skills in project management and team leadership.
Educational Background in Biomedical Engineering
Joshita Majumdar earned her Bachelor's degree in Biomedical/Medical Engineering from Manipal Institute of Technology, completing her studies from 2008 to 2012. She further advanced her education by obtaining a Master's degree in Biomedical Engineering from Carnegie Mellon University, where she studied from 2012 to 2014.
Research and Teaching Roles at Carnegie Mellon University
Joshita held multiple roles at Carnegie Mellon University, including Research Assistant and Teaching Assistant from 2013 to 2014. In these positions, she contributed to the Center for Bio Image Informatics and assisted in teaching, demonstrating her commitment to academic excellence. Additionally, she served as a Grader for the course 'Numerical Methods' in the Department of Mathematics during the same period.
Regulatory and Product Development Expertise
In her current role, Joshita provides regulatory guidance for product development, preparing and submitting regulatory file applications and supporting documentation. She develops regulatory strategies for new and modified medical devices, ensuring compliance throughout the product lifecycle. Her work includes designing and testing prototypes to optimize product design and improve clinical workflow efficiency.