Srushti C.
About Srushti C.
Srushti C. is a Senior Systems Engineer with extensive experience in the medical device and in vitro diagnostics industry. She has held various engineering roles at Roche, Coeo Labs, and Philips, and holds a Master's degree in Bioengineering from the University of Michigan.
Current Role at Baebies
Srushti C. serves as a Senior Systems Engineer at Baebies, a position she has held since 2021. In this role, she focuses on new product introduction and on-market product sustainment within the medical device and in vitro diagnostics sectors. Her responsibilities include leading cross-functional product development activities, applying systems thinking, and utilizing problem-solving skills to drive healthcare innovation.
Previous Experience at Roche
Prior to her current role, Srushti worked at Roche for three years, where she held two positions. She served as Systems Engineer II from 2020 to 2021 and as Systems Engineer I from 2018 to 2020. Both roles were based in San Jose, California, where she contributed to various engineering projects within the medical device industry.
Experience at Coeo Labs Pvt. Ltd.
Srushti began her career at Coeo Labs Pvt. Ltd., where she worked as a Product Development Engineer from 2015 to 2016 for 11 months in Bangalore, India. She also held the position of Trainee Engineer at the same company from 2014 to 2015 for 8 months. Her work involved product development activities that laid the foundation for her expertise in engineering.
Educational Background
Srushti holds a Bachelor of Engineering (B.E.) in Biomedical/Medical Engineering from Dayananda Sagar Institutions. She furthered her education by obtaining a Master's degree in Bioengineering and Biomedical Engineering from the University of Michigan - Rackham Graduate School. This academic background supports her technical expertise in the medical device field.
Certifications and Regulatory Knowledge
Srushti is certified in Systems Engineering by INCOSE. She is familiar with a variety of regulations and standards relevant to the medical device industry, including MDR, 21 CFR 820, IVDR, CAP/CLIA, ISO 13485, IEC-60601-1, ISO 14971, and IEC 62304. This knowledge enhances her ability to navigate complex regulatory environments in her engineering roles.