Ritika Roy
About Ritika Roy
Ritika Roy is the Manager of QA Compliance at Bristol Myers Squibb in Warren, New Jersey, with extensive experience in quality management and compliance within the biotechnology industry.
Manager, QA Compliance at Bristol Myers Squibb
Ritika Roy currently holds the position of Manager, QA Compliance at Bristol Myers Squibb in Warren, New Jersey, United States. Her responsibilities likely involve managing quality assurance protocols and ensuring compliance with regulatory standards within the company’s operations.
Previous Roles at Bristol Myers Squibb
Before her current role, Ritika Roy was a Senior Specialist in Manufacturing Compliance for Clinical CAR-T at Bristol Myers Squibb from 2020 to 2023. She spent three years in Warren, New Jersey, focusing on maintaining and enhancing the compliance standards in clinical CAR-T manufacturing processes.
Experience at Novartis
Ritika Roy worked at Novartis in Morris Plains, New Jersey, first as a QA Specialist for Batch Release from 2019 to 2020, and subsequently as a GMP Officer in QA Operations in 2020. In these roles, she focused on ensuring product quality and adherence to Good Manufacturing Practices, each for periods under a year.
Quality Engineer at Ortho Clinical Diagnostics
In 2018, Ritika Roy served as a Quality Engineer II at Ortho Clinical Diagnostics in Raritan, New Jersey for eight months. This role involved responsibilities related to quality engineering and compliance in clinical diagnostics.
QC Operations at Roche
Ritika Roy's career at Roche spanned nearly four years in Branchburg, New Jersey, where she began as a Lab Tech in QC Operations from 2014 to 2017 and was promoted to Sr. Lab Tech, QC Operations until 2018. She contributed significantly to quality control and operational excellence in these roles.
Academic Background
Ritika Roy pursued her studies at Rutgers University, where she obtained a Bachelor of Science (B.S.) in Biotechnology. She furthered her education with a Master of Business and Science (M.B.S.) focused on Biotechnology and Genomics. Her academic background laid a strong foundation for her career in quality management in the biotechnology sector.
Technical Expertise
Ritika Roy has developed extensive expertise in Quality Management and Compliance within the biotechnology industry. She specializes in GMP (Good Manufacturing Practices) and technical writing. Her career journey reflects her in-depth knowledge and experience in these domains.
Location
Ritika Roy is currently based in the New York City Metropolitan Area, contributing her expertise in quality assurance and compliance within the biotechnology industry.