Shefali Pandya Email & Phone Number | As a Regulatory Affairs and Submission Management Associate at Tata Consultancy Services, I work with Janssen Pharmaceuticals to ensure the compliance and quality of their drug products and labels. I have a Master's degree in Pharmaceutical Chemistry from Manipal Academy of Higher Education, and a Bachelor of Pharmacy from Rajasthan University of Health Sciences, Jaipur. I have total 5 years of experience in the field of regulatory affairs, having worked with Bristol Myers Squibb as a Regulatory Affairs Associate and a Junior Regulatory Affairs Associate at Parexel. I have developed skills in regulatory Submission including SNDS, NC and other post approval life cycle management submissions and have contributed to the successful submission and approval of multiple drug applications in various markets. I am passionate about applying my knowledge and expertise to support the development and delivery of innovative and safe medicines for patients.

Shefali Pandya

As a Regulatory Affairs and Submission Management Associate at Tata Consultancy Services, I work wit...
Mississauga, Mississauga, Canada

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Shefali Pandya’s Email shefali.pandya@tcs.com

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Shefali Pandya’s Location Mississauga, Mississauga, Canada

Shefali Pandya’s Current Industry Baxter International

Shefali Pandya’s Prior Industry Tata Consultancy Services | Parexel | Eurofins Advinus

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Shefali Pandya is a As a Regulatory Affairs and Submission Management Associate at Tata Consultancy Services, I work with Janssen Pharmaceuticals to ensure the compliance and quality of their drug products and labels. I have a Master's degree in Pharmaceutical Chemistry from Manipal Academy of Higher Education, and a Bachelor of Pharmacy from Rajasthan University of Health Sciences, Jaipur. I have total 5 years of experience in the field of regulatory affairs, having worked with Bristol Myers Squibb as a Regulatory Affairs Associate and a Junior Regulatory Affairs Associate at Parexel. I have developed skills in regulatory Submission including SNDS, NC and other post approval life cycle management submissions and have contributed to the successful submission and approval of multiple drug applications in various markets. I am passionate about applying my knowledge and expertise to support the development and delivery of innovative and safe medicines for patients.