Ranjit Chavan
About Ranjit Chavan
Ranjit Chavan is the Director of Software R&D at Boston Scientific, with extensive experience in software engineering and medical device connectivity.
Current Role at Boston Scientific
Ranjit Chavan is currently serving as the Director of Software R&D at Boston Scientific in Pune, Maharashtra, India. His tenure as Director began in 2023. Prior to this role, he held the position of Associate Director, Software, from 2022. In these roles, he is responsible for overseeing the research and development of software solutions integral to Boston Scientific's medical devices.
Previous Roles at Boston Scientific
Before his current role, Ranjit Chavan worked as the Senior Software Engineering Manager at Boston Scientific from 2017 to 2022 in Gurugram. His responsibilities included managing engineering teams and ensuring the delivery of high-quality software products. He also served as the Software Engineering Manager from 2016 to 2017 in Gurgaon, where he focused on leading software development projects for medical devices.
Other Professional Experience
Ranjit Chavan has a diverse background spanning various roles in different companies. He was an Associate Director at IGATE from 2014 to 2016 and a Senior Technology Architect at Infosys from 2012 to 2014, both in the Pune Area. Earlier in his career, he worked at Patni Computer Systems as a Program Manager from 2001 to 2012 and at DYP College of Engineering as a Lecturer for C and C++ from 1999 to 2000.
Education
Ranjit Chavan holds a Bachelor of Engineering (BE) degree in Mechanical Engineering from Walchand College of Engineering, where he studied from 1992 to 1996. His educational background laid the foundation for his extensive career in software engineering and medical device connectivity.
Technical Expertise and Skills
Ranjit Chavan specializes in software design and development using programming languages such as C#, C++, VC++, and VC .Net. He is adept in Object-Oriented Analysis and Design methodologies. Additionally, he is a trained ISO 13485 auditor and possesses in-depth knowledge of FDA regulations related to medical product development. His expertise also includes medical device connectivity and standards like IHE and HL7.