Shubhashish Mukhopadyay
About Shubhashish Mukhopadyay
Shubhashish Mukhopadyay is a Senior Scientist with extensive experience in biotechnology and pharmaceuticals. He has worked at the University of Oxford since 2011 and currently holds a position at Exscientia, with a strong background in GMP analysis, quality control, and regulatory affairs.
Work at Exscientia
Shubhashish Mukhopadyay has been employed at Exscientia as a Senior Scientist since 2022. In this role, he focuses on advancing the company's research initiatives within the biotechnology sector. His responsibilities include conducting experiments, analyzing data, and collaborating with cross-functional teams to drive innovation in drug discovery and development.
Current Role at University of Oxford
Since 2011, Shubhashish Mukhopadyay has served as a Research Scientist at the University of Oxford. Over the past 13 years, he has contributed to various research projects, leveraging his expertise in pharmacology and biotechnology. His work involves conducting high-level research and contributing to the academic community within the university.
Education and Expertise
Shubhashish Mukhopadyay earned a Master of Science in Pharmacology and Biotechnology from Sheffield Hallam University, where he studied from 2004 to 2006. His educational background provides a solid foundation for his extensive experience in the biotechnology and pharmaceutical industries, particularly in areas such as GMP analysis and quality control.
Professional Background
Shubhashish Mukhopadyay has a diverse professional background. He began his career at Claris Lifesciences Limited as an International Regulatory Affairs Assistant from 2003 to 2004. He then worked as an R&D Analyst at RB from 2006 to 2008. Additionally, he gained customer service experience at NatWest Bank from 2010 to 2011 before joining the University of Oxford.
Regulatory Affairs and Quality Control Experience
With over a decade of experience in GMP analysis and quality control, Shubhashish Mukhopadyay possesses a strong background in regulatory affairs. His expertise ensures compliance with high-quality standards in the pharmaceutical sector, contributing to the development of safe and effective biopharmaceutical products.