Pranitha supports the QA/RA team while working closely with the Lab Operations team contributing across both quality and operational activities. Her role focuses on ensuring that quality and regulatory requirements are consistently met, helping teams deliver projects in a compliant and efficient way.
“I’ve always been drawn to the medical device sector and I’m passionate about working in regulated environments, where quality and compliance directly support innovative technologies that improve patient lives.”
“I feel proud to be part of a field and a company like Team Consulting that is focused on improving patient outcomes through innovation and high-quality standards.”
Pranitha has a master’s degree in biotechnology from Kakatiya University. She has over 12 years of experience across pharmaceutical, medical device and healthcare industries, with a strong focus on Quality and Device Regulatory Affairs (QARA), including IVDR clinical projects.