Therese Dahlsköld
About Therese Dahlsköld
Therese Dahlsköld is a Regulatory Affairs Associate at Bristol-Myers Squibb with over 12 years of experience in regulatory affairs and project coordination within the pharmaceutical industry.
Current Role at Bristol-Myers Squibb
Therese Dahlsköld is currently working as a Regulatory Affairs Associate at Bristol-Myers Squibb. In this role, she is responsible for ensuring compliance with various regulatory standards and guidelines. Her position involves coordinating with different departments to manage regulatory submissions and maintain up-to-date knowledge on regulations that affect the pharmaceutical industry. This role continues her long tenure with the company, where she brings her expertise to support the organization's regulatory needs.
Previous Positions at Bristol-Myers Squibb
Before becoming a Regulatory Affairs Associate, Therese Dahlsköld held multiple roles within Bristol-Myers Squibb. She served as a Regional Regulatory Assistant from 2011 to 2015 in New York, where she specialized in regional compliance activities. Prior to that, she worked as a Project Coordinator from 2010 to 2011, focusing on project management tasks. Her diverse experience at the company highlights her adaptability and comprehensive understanding of both project coordination and regulatory affairs.
Education Background
Therese Dahlsköld studied at Florida Southern College, where she completed a Bachelor of Business Administration. Her academic tenure lasted from 2006 to 2010, providing her with a fundamental understanding of business principles that she has applied throughout her career in the pharmaceutical industry. This educational background has been instrumental in her proficiency in managing complex regulatory and project coordination tasks.
Experience in the Pharmaceutical Industry
Therese Dahlsköld has accumulated over 12 years of experience in regulatory affairs and project coordination within the pharmaceutical industry. Her extensive career at Bristol-Myers Squibb has seen her transition through various roles, building a profound understanding of both local and regional regulatory requirements. Her ability to navigate complex regulatory environments and contribute to large-scale projects underscores her valued presence in the industry.