ÂÜÀòÂÒÂ×

Sumit Sah is a Validation Engineer at Sigilon Therapeutics, Inc., with extensive experience in computer systems validation to comply with FDA regulations. Responsibilities include authoring and reviewing key validation documents such as Validation Plans, GxP assessments, Risk assessments, and Test/Validation summary reports, along with writing User Requirements Specifications (URS) and Functional Requirements Specifications (FRS). Prior to this role, Sumit worked as a CSV Engineer at 3Analytics India Private Limited, where contributions included creating GxP assessments and participating in Risk assessment preparations. Earlier in the career, Sumit interned in Quality Control at Micro Labs Ltd., focusing on the analysis of finished products and preparing protocols and summary reports. Sumit holds a Bachelor's degree in Microbiology from St. Xavier's College, Maitighar.