Shikha Jash
About Shikha Jash
Shikha Jash is a Specialist in CAR-T Operations Scheduling at Bristol Myers Squibb with extensive experience in the pharmaceutical industry, including roles at Janssen, Eli Lilly, Abbvie, and Limited Brands.
Company
Shikha Jash is currently employed at Bristol Myers Squibb in the United States. In her role as a Specialist in CAR-T Operations Scheduling, she manages the logistical and operational aspects of CAR-T cell therapy. Bristol Myers Squibb is a global biopharmaceutical company focused on discovering, developing, and delivering innovative medicines.
Title and Role at Bristol Myers Squibb
Shikha Jash serves as a Specialist, CAR-T Operations Scheduler at Bristol Myers Squibb. Her responsibilities include coordinating and managing the operational workflow for CAR-T cell therapy. This role requires meticulous planning and scheduling to ensure timely and efficient production and delivery of CAR-T treatments.
Professional Experience and Background
Before joining Bristol Myers Squibb, Shikha Jash worked at The Janssen Pharmaceutical Companies of Johnson & Johnson as a Lead CAR-T Manufacturing Associate from 2019 to 2021 in Raritan, New Jersey. She also served as a Cell Culture Tech at Eli Lilly and Company from 2016 to 2019 in the Greater New York City Area. Prior to that, she was a Production Technician at Abbvie (Lifecell) in New Jersey for 8 months in 2015 to 2016. Her career began at Limited Brands, where she worked as an Associate from 2011 to 2015.
Education and Expertise
Shikha Jash earned a Bachelor's Degree in Biotechnology from Rutgers University-New Brunswick, where she studied from 2014 to 2017. She also obtained an Associate's Degree in Biotechnology and General Biology from Raritan Valley Community College, where she studied from 2012 to 2014. Her educational background provided her with a strong foundation in biotechnology, reinforced by practical experiences in various roles.
Specialized Skills and Competencies
Shikha Jash possesses specialized skills in Good Tissue Practice (cGTP), Good Documentation Practice (GDP), and Good Manufacturing Practice (GMP). She has strong expertise in Trend Analysis and is adept at using Microsoft Word for documentation and reporting tasks. Her robust communication skills facilitate effective collaboration and coordination within a pharmaceutical setting, ensuring high standards of quality and compliance are maintained.