Pavan Jhutti, Rac

Pavan Jhutti, Rac

Associate Director, Regulatory Affairs Cmc @ BeiGene

About Pavan Jhutti, Rac

Pavan Jhutti is the Associate Director of Regulatory Affairs CMC at BeiGene, with over 20 years of experience in the pharmaceutical industry.

Title and Role

Pavan Jhutti holds the position of Associate Director, Regulatory Affairs CMC at BeiGene. In this role, Pavan is responsible for regulatory strategies and submissions related to Chemistry, Manufacturing, and Controls (CMC) for the company's pharmaceutical products. This position involves navigating complex regulatory environments to ensure that BeiGene's products meet all necessary standards.

Career at BeiGene

Pavan Jhutti joined BeiGene in December 2020 as the Associate Director of Regulatory Affairs CMC. With expertise in regulatory strategies, Pavan plays a key role in ensuring that BeiGene’s pharmaceutical products comply with industry regulations. This includes managing regulatory submissions, liaising with regulatory agencies, and staying updated on regulatory changes and their implications for the company.

Previous Experience at BioMarin Pharmaceutical Inc.

Before joining BeiGene, Pavan Jhutti worked at BioMarin Pharmaceutical Inc. as a Regulatory Affairs Senior Manager from 2008 to 2020. Over 12 years, Pavan was involved in regulatory affairs, focusing on the approval and compliance of new drugs. This role required in-depth knowledge of global regulatory requirements and the ability to manage complex submissions.

Early Career in Formulation and Process Development

Pavan Jhutti began his career in the pharmaceutical industry with Dow Pharmaceutical Sciences, Inc, where he served as a Formulation & Process Development Chemist from 2000 to 2008. During this period, Pavan worked on developing and optimizing pharmaceutical formulations and processes. This experience provided a strong foundation in pharmaceutical chemistry and manufacturing.

Educational Background

Pavan Jhutti studied at the University of California, Davis. The education received from UC Davis has played a crucial role in equipping Pavan with the knowledge and skills necessary for a successful career in the pharmaceutical industry. Pavan's academic background laid the foundation for his expertise in regulatory affairs, formulation chemistry, and quality control.

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