Shilpi Rajoria
About Shilpi Rajoria
Shilpi Rajoria is the Sr. QC Manager CAR T at Bristol Myers Squibb in Summit, New Jersey, specializing in flow cytometry-based testing and QC data management.
Current Title and Role
Shilpi Rajoria holds the position of Senior QC Manager CAR T at Bristol Myers Squibb, located in Summit, New Jersey. In this role, she leads data review and management for the Quality Control (QC) department and acts as a Subject Matter Expert (SME) for QC Flow during regulatory inspections. Shilpi is also responsible for the validation and requalification support within the QC Flow Cytometry department.
Previous Work Experience
Prior to her current role, Shilpi Rajoria has accumulated extensive experience in the field of quality control and research. She served as Manager CAR T at Bristol Myers Squibb from 2018 to 2020 and as Senior QC Scientist at Celgene from 2017 to 2018. Shilpi also worked as an Analyst at LabCorp Clinical Trials from 2016 to 2017, and held postdoctoral positions at Rutgers University and Albany Medical Center, focusing on oncology and cancer biology.
Educational Background
Shilpi Rajoria completed her Doctor of Philosophy (PhD) in Oncology and Cancer Biology from New York Medical College. She also holds a Master of Science (MSc) degree in Biotechnology from the University of Rajasthan. Her educational background has provided a strong foundation in biochemical and cellular sciences, enabling her to excel in her subsequent professional roles.
Specializations and Expertise
Shilpi Rajoria specializes in Flow Cytometry-based testing, including in-process sample testing, final drug product testing, and stability testing. She oversees critical reagent testing and qualification and provides training and other essential support within the QC department. Her expertise ensures the highest standards of quality control in her projects.
Professional Responsibilities
In her role as Senior QC Manager CAR T, Shilpi Rajoria is responsible for the oversight and validation of various QC processes. She leads the department in data review, acts as a Subject Matter Expert (SME) during regulatory inspections, and ensures that all testing and validation processes meet stringent quality standards. Additionally, she supports critical reagent testing and qualifications, contributing significantly to the department's operational excellence.