Supriya Paratkar
About Supriya Paratkar
Supriya Paratkar is a Documentation Analyst at Bristol Myers Squibb in New Jersey, with extensive experience in regulatory affairs and project management in the pharmaceutical industry.
Current Position at Bristol Myers Squibb
Supriya Paratkar currently holds the position of Documentation Analyst at Bristol Myers Squibb in New Jersey, United States. In this role, she is responsible for managing and maintaining accurate documentation essential for regulatory compliance. Her work ensures that all records meet the industry's stringent guidelines and contribute to the seamless approval of products.
Previous Role at Novartis
From 2019 to 2021, Supriya Paratkar worked as a Regulatory Submissions Coordinator at Novartis in East Hanover, New Jersey. During her tenure, she coordinated the submission processes, ensuring that regulatory documents were prepared, reviewed, and submitted in compliance with various regulatory authorities. Her role contributed to the successful market entry and maintenance of Novartis products.
Education in Biotechnology
Supriya Paratkar studied Biotechnology at Mumbai University, where she earned both her Bachelor's degree (2008-2011) and Master's degree (2011-2013). Her educational background has equipped her with the technical knowledge and skills required to excel in regulatory affairs within the pharmaceutical industry.
Professional Experience in Regulatory Affairs
Supriya Paratkar has extensive experience in regulatory affairs across various organizations. She worked as a Regulatory Associate at Syner-G Pharma Consulting, LLC for three months in 2018 in Rahway, New Jersey. Earlier, she served as a Regulatory Affairs Officer at Indoco Remedies Ltd. for five months in 2016 and as a Regulatory Affairs Associate at Cipla Ltd. from 2014 to 2016 in Mumbai. Her professional journey began with roles as a Project Trainee at Glenmark Pharmaceuticals for 11 months in 2014 and as an Intern at Piramal LifeSciences Limited for 11 months in 2012, both in Mumbai.
Specialized Certification and Expertise
Supriya Paratkar holds a Regulatory Affairs Certificate (RAC) specializing in Pharmaceuticals. Her expertise encompasses life cycle management of existing products for the South East Asia market, change control assessment, and renewals. Additionally, she has experience handling submissions for regulatory bodies like the Therapeutic Goods Administration (TGA) and Health Canada, demonstrating her proficiency in international regulatory standards.