Parita Varma Ms, Rac Us
About Parita Varma Ms, Rac Us
Parita Varma is a Senior Manager II Global Regulatory CMC Biologics at Bristol Myers Squibb in Greater Boston with extensive experience in regulatory affairs.
Title
Parita Varma is the Senior Manager II Global Regulatory CMC Biologics at Bristol Myers Squibb in Greater Boston.
Company
Parita Varma is currently employed at Bristol Myers Squibb where she holds the position of Senior Manager II Global Regulatory CMC Biologics.
Professional Experience
Parita Varma has a robust professional background in regulatory affairs. She served as Regulatory Affairs Manager at Amgen from 2016 to 2022 in Greater Boston. Prior to that, she was Regulatory Affairs Specialist II at Sanofi Genzyme in 2016 for three months. In 2015, she worked as Regulatory Affairs Specialist at CTI BioPharma in Greater Seattle for five months. Earlier in her career, she was an International Regulatory Affairs Specialist at Claris Lifesciences Limited in Ahmedabad from 2012 to 2014. She also completed internships as an Analytical Intern at Dishman in 2012 for three months and as a Manufacturing Intern at Zydus Group in 2008 for one month in Ahmedabad, India.
Education and Expertise
Parita Varma holds a Master's Degree in Regulatory Affairs in Drugs, Biologics, and Medical Devices from Northeastern University, where she studied from 2014 to 2016. She earned her M. Pharm in Pharmaceutical Analysis from Gujarat Forensic Sciences University between 2010 and 2012. Additionally, she graduated with a Bachelor of Pharmacy (B.Pharm.) from Savitribai Phule Pune University, where she studied from 2006 to 2010.
Regulatory Submissions
Parita Varma is skilled in handling regulatory submissions for both FDA and EMA, covering Modules 1-5. She combines her patience and determination to effectively solve complex regulatory problems and meet strict regulatory deadlines.