Shilpa P. Thomsen

Shilpa P. Thomsen

Manager, European Regulatory Procedural Strategy @ Bristol Myers Squibb

About Shilpa P. Thomsen

Shilpa P. Thomsen is a Manager of European Regulatory Procedural Strategy at Bristol Myers Squibb with extensive experience in regulatory affairs, particularly in oncology and rare diseases.

Title and Current Role

Shilpa P. Thomsen currently serves as the Manager of European Regulatory Procedural Strategy at Bristol Myers Squibb. In this role, she is responsible for developing and implementing regulatory strategies to ensure compliance with European regulations. Her involvement focuses on procedural aspects, aiming to facilitate efficient and effective regulatory submissions and approvals.

Previous Experience at Ipsen

Before joining Bristol Myers Squibb, Shilpa Thomsen worked at Ipsen in several capacities. She held the position of Global Regulatory Affairs Specialist (Rare Disease) through a secondment in 2023 for ten months. From 2021 to 2023, she served as Senior Regulatory Affairs Officer for the UK and Ireland, specifically in the oncology sector. She initially joined Ipsen in 2020 as a Regulatory Affairs Officer based in Slough, England, where she worked for eight months.

Early Career at Perrigo Company and Pfizer

Shilpa Thomsen started her regulatory affairs career at Perrigo Company plc, where she worked as a Regulatory Affairs Associate for the UK and Ireland from 2018 to 2020. During this period, she was based in London, United Kingdom. Prior to Perrigo, she gained experience in supply chain and marketing quality operations at Pfizer, where she served as a Supply Chain and Marketing Quality Operations Executive for six months in 2018 in Tadworth.

Educational Background in Medicinal Chemistry

Shilpa Thomsen's formal education includes a Master of Science (MS) in Medicinal Chemistry from the University of Birmingham and a Bachelor of Science (BS) from Kingston University. She completed her secondary education at Coloma Convent Girls' School. Her academic background provides a strong foundation for her professional roles in regulatory affairs, particularly within the pharmaceutical and biotechnology sectors.

Expertise in Regulatory Affairs and Oncology

Shilpa Thomsen has extensive expertise in regulatory affairs with a specific focus on the oncology sector. Her experience includes developing regulatory strategies and ensuring compliance within highly regulated environments. She has also gained specialized knowledge in handling rare diseases through her secondment at Ipsen, adding a significant dimension to her professional portfolio.

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