Brinda Sukhadia
About Brinda Sukhadia
Brinda Sukhadia is a Senior Specialist in Systems Training at Bristol Myers Squibb in Summit, New Jersey, with a background in microbiology and quality control.
Title and Current Position
Brinda Sukhadia holds the position of Senior Specialist, Systems Training at Bristol Myers Squibb, based in Summit, New Jersey, United States. In this role, she contributes to the development and execution of training programs, ensuring adherence to industry standards and regulatory requirements.
Previous Experience in Training and Development
Prior to her current role, Brinda Sukhadia served as a Training & Development Associate Specialist at Bristol Myers Squibb for 10 months from 2020 to 2021. During her tenure, she facilitated various training initiatives, supporting the development and implementation of comprehensive training programs.
Professional Experience in Microbiology and Quality Control
Brinda Sukhadia has extensive experience in the fields of microbiology and quality control. She worked as a Scientist, Microbiology Data Reviewer at Immunomedics for 5 months from 2019 to 2020, and as an Associate Scientist at Celgene for 1 year from 2018 to 2019. Additionally, she held the role of Research Associate, QC at Celgene in 2018 for 7 months and was a Senior QC Microbiologist at Aspire Pharmaceuticals from 2017 to 2018 for 9 months. Her experience also includes positions such as Senior Microbiologist at Loricon Testing Svc and Microbiologist at Qualimax LLC and Valspar.
Educational Background in Biotechnology and Pharmacy
Brinda Sukhadia earned her Master of Science (MS) in Biotechnology from Roosevelt University, where she studied from 2011 to 2013. She also holds a Bachelor of Pharmacy (B.Pharm.) from ROFEL College of Pharmacy in India, where she studied Pharmacy, Pharmaceutical Sciences, and Administration from 2002 to 2006.
Expertise in Compliance and Quality Documentation
Brinda Sukhadia has a proven track record in authoring and reviewing numerous reports and procedures to ensure compliance with cGMP and cGLP standards. Her excellent proofreading skills have significantly contributed to the accuracy and quality of documentation. Known for her diligence and dependability, she excels in working independently as well as collaboratively within team environments.