Harjit Banga
About Harjit Banga
Harjit Banga is the Vice President of Global Scientific and Regulatory Documentation and Writing at Bristol-Myers Squibb, with over 30 years of experience in regulatory documentation and drug regulatory affairs.
Current Role at Bristol-Myers Squibb
Harjit Banga currently holds the position of Vice President, Global Scientific and Regulatory Documentation and Writing at Bristol-Myers Squibb. Positioned in New Jersey, United States, he is responsible for overseeing the company's global documentation and scientific communication efforts. His role involves ensuring that all regulatory materials align with industry standards and regulatory requirements.
Previous Experience at Bristol-Myers Squibb
Before his current role, Harjit Banga worked as Executive Director, Global Regulatory Documentation at Bristol-Myers Squibb from 2001 to 2014. In this capacity, he spent 13 years managing the regulatory documentation processes for the company, contributing significantly to its regulatory affairs strategy. His long tenure with the company showcases his expertise and dedication in this specialized field.
Experience at Roche
Harjit Banga has extensive international experience from his time at Roche. He served as International Documentation Manager, Regulatory Documentation and Drug Regulatory Affairs in Switzerland from 1993 to 2001. Prior to that, he worked as an Associate Research Investigator in Cardiovascular and Metabolic Research from 1990 to 1993. His work at Roche provided him with a robust foundation in regulatory documentation and medical research.
Educational Background
Harjit Banga's academic background is distinguished by his studies in biochemistry. He studied at Harvard Medical School for a year from 1985 to 1986. He also studied at MS University, Baroda (India), earning multiple degrees: Master of Science, Doctorates, Masters, and Doctor of Philosophy in Biochemistry, spanning from 1977 to 1985. This strong educational foundation underpins his expertise in the scientific and regulatory fields.
Extensive Experience in Regulatory Documentation
With over 30 years of experience in regulatory documentation and drug regulatory affairs, Harjit Banga offers significant expertise in this domain. This includes his roles both at Roche and Bristol-Myers Squibb, where he has specialized in managing complex regulatory documentation processes across different geographic regions. His comprehensive background positions him as a subject matter expert in regulatory affairs and scientific documentation.