Catherine Dorion
About Catherine Dorion
Catherine Dorion is the Senior Manager of Regulatory Affairs for Immunology and Fibrosis at Bristol Myers Squibb in Montreal, Quebec, Canada, with over 20 years of experience in the pharmaceutical industry.
Title
Catherine Dorion holds the position of Senior Manager Regulatory Affairs, specializing in Immunology and Fibrosis, at Bristol Myers Squibb. She operates from Montreal, Quebec, Canada.
Current Role at Bristol Myers Squibb
Catherine Dorion currently serves as the Senior Manager of Regulatory Affairs at Bristol Myers Squibb, focusing on Immunology and Fibrosis. Her role involves managing regulatory submissions and ensuring compliance with regulatory requirements for pharmaceutical products within these therapeutic areas.
Previous Experience at Prometic
From 2015 to 2021, Catherine Dorion was the Director of Regulatory Affairs at Prometic. During her tenure, she provided strategic regulatory direction and oversaw the preparation and submission of regulatory documents, ensuring compliance with international standards.
Experience at Jubilant DraxImage
Between 2009 and 2015, Catherine Dorion held dual roles as Senior Project Leader and Supervisor of Regulatory Affairs at Jubilant DraxImage. Here, she led regulatory projects and supervised regulatory activities, enhancing the company's regulatory strategies and submissions.
Career at Bristol-Myers Squibb
Catherine Dorion worked as a Senior Associate in Regulatory Affairs at Bristol-Myers Squibb from 2001 to 2009. During these eight years, she gained foundational experience in regulatory submissions and compliance, contributing to her expertise in the field.
Expertise in Regulatory Affairs
With over 20 years of experience in the pharmaceutical industry, Catherine Dorion specializes in regulatory affairs, particularly for immunology and fibrosis. Her extensive experience includes leadership roles, project management, and supervision, emphasizing regulatory compliance and effective submissions.