Padmavathi S is a motivated and goal-oriented Senior Software Engineer at Quest Global, specializing in Medical Device Regulation. With 3 years of experience in Regulatory Affairs at Tata Elxsi, Padmavathi has expertise in ensuring compliance with EU MDR and US FDA regulations, as well as in risk management and design control documents. Padmavathi holds a Bachelor of Engineering in Biomedical/Medical Engineering and completed advanced training in Biomedical applications.
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