Srividya Balasubramanian
About Srividya Balasubramanian
Srividya Balasubramanian is a Quality Systems Associate at Bristol Myers Squibb with a background in biotechnology and biotherapeutics, and experience in quality control and teaching.
Title and Current Position
Srividya Balasubramanian currently holds the position of Quality Systems Associate at Bristol Myers Squibb. In this role, she focuses on maintaining and improving quality standards within the company’s operational framework, adhering to industry regulations and guidelines.
Professional Experience at Rajiv Gandhi Institute
Srividya Balasubramanian worked as Visiting Faculty at the Rajiv Gandhi Institute of Information Technology and Biotechnology in Pune Area, India. She served from 2018 to 2019 for a duration of 4 months, contributing to the academic and professional development of students in the field of biotechnology.
Career at Serum Institute of India
Srividya Balasubramanian gained substantial professional experience at the Serum Institute of India Pvt. Ltd. Initially, she worked as a Summer Intern in 2016 for 2 months followed by a role as a Quality Control Analyst in 2018 for 5 months. Her contributions were in line with cGLP and cGMP standards, performing critical laboratory and quality control tasks.
Educational Background
Srividya Balasubramanian holds a Master's degree in Biotherapeutics and Business from UCD Michael Smurfit Graduate Business School, earned in 2020. She also obtained a postgraduate diploma in Bioinformatics from Rajiv Gandhi Institute of Information Technology and Biotechnology, Pune, in 2018. Prior to this, she graduated with a Bachelor's degree in Biotechnology from the same institution in 2017.
Technical Skills and Expertise
With over 3 years of laboratory experience in biochemistry, molecular biology, and microbiology, Srividya Balasubramanian is well-versed in cGLP and cGMP standards. She is also familiar with EU regulatory guidelines. Her skills include SOP review and verification per cGMP standards, making her proficient in documentation procedures and regulatory compliance.