Sai T Dharwada, M.Sc., Qac

Clinical Compliance Associate @ Travere Therapeutics

About Sai T Dharwada, M.Sc., Qac

Sai T Dharwada is a Clinical Compliance Associate at Travere Therapeutics with a background in pharmaceutical regulatory affairs and quality operations. He holds a Master of Science from The University of British Columbia and has experience in research and quality assurance roles across various organizations.

Work at Travere Therapeutics

Sai T Dharwada has been employed at Travere Therapeutics as a Clinical Compliance Associate since 2020. In this role, he is responsible for ensuring that clinical operations adhere to regulatory standards and internal policies. His work contributes to the overall compliance framework of the organization, supporting the development and approval of therapeutic products.

Education and Expertise

Sai T Dharwada holds a Master of Science degree from The University of British Columbia, which he completed from 2012 to 2015. He also has a Bachelor of Science degree from the University of Windsor, obtained between 2009 and 2012. In addition, he studied Pharmaceutical Regulatory Affairs and Quality Operations at Seneca College from 2019 to 2020. His education is complemented by further studies at Harvard T.H. Chan School of Public Health in 2022.

Background

Before joining Travere Therapeutics, Sai T Dharwada worked as a Research Technician at the University of Toronto from 2016 to 2018. He also held the position of Process Analyst II in Analytical Quality Assurance at Abbott for three months in 2020. Additionally, he gained experience as a Quality Assurance and Compliance Associate (Co-op) at Mint Pharmaceuticals from 2019 to 2020.

Professional Experience

Sai T Dharwada has diverse professional experience in clinical compliance and quality assurance. His role at Abbott involved analytical quality assurance, while his position at Mint Pharmaceuticals focused on quality assurance and compliance. This breadth of experience has equipped him with a solid understanding of regulatory requirements and quality operations within the pharmaceutical industry.

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