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Ramesh Kuril has a diverse and extensive work experience in the field of regulatory affairs. Ramesh started their career in 2003 at Claris lifesciences ltd as a Biotech Project Manager, where they worked until 2005. Ramesh then joined Intas Biopharmaceuticals in 2005 as a Quality Manager, where they stayed until 2007.

In 2008, Ramesh joined Serum Institute of India Limited as a Regulatory Affairs Biologics professional. During their time there, they handled various products registrations in India, Europe, and other markets. Ramesh provided technical and scientific inputs in the preparation, registration, and maintenance of biological and recombinant products. Ramesh also prepared multiple modules and complete CMC quality sections on vaccines and recombinant products. Ramesh successfully submitted several dossiers for registration in different markets and ensured compliance with regulatory requirements. Ramesh also managed post-approval changes for various regulatory authorities.

From 2011 to 2017, Ramesh worked at BioGenomics Ltd., initially as a Manager Regulatory Affairs and later as a Senior Manager Regulatory Affairs.

In 2017, Ramesh joined Enzene Biosciences Ltd. as an Assistant General Manager Regulatory Affairs. Ramesh was later promoted to Deputy General Manager and then to their current role as Regulatory Affairs General Manager.

Throughout their career, Ramesh Kuril has gained extensive experience and expertise in regulatory affairs, particularly in product registrations, dossier preparation, compliance, and post-approval changes.

Ramesh Kuril completed their Higher Secondary education at Indian Rayon School in Veraval from 1984 to 1998. Ramesh then pursued their Bachelors in Biotechnology and Chemistry, as well as their Masters in Biochemistry, from Savitribai Phule Pune University from 1998 to 2003. Ramesh's academic focus has been on the fields of Biotechnology and Biochemistry.