Huguette Stephanie Bodo Kamga
About Huguette Stephanie Bodo Kamga
Huguette Stephanie Bodo Kamga is the Executive Director of Regulatory Affairs at Alkermes in Waltham, MA, with over 15 years of experience in the pharmaceutical industry.
Current Role at Alkermes
Huguette Stephanie Bodo Kamga serves as the Executive Director of Regulatory Affairs at Alkermes, based in Waltham, MA. In this capacity, she oversees the regulatory strategy and operations, ensuring that all products comply with global regulatory standards. Her role involves collaborating with various internal departments and external bodies to maintain compliance and facilitate the approval of new pharmaceuticals.
Previous Experience at Ipsen US
Before joining Alkermes, Huguette Stephanie Bodo Kamga worked at Ipsen US as the Senior Director of Global Regulatory Affairs. She spent three years in this role from 2018 to 2021, located at 650 East Kendall Street, Cambridge, MA. Her responsibilities included leading global regulatory initiatives and ensuring the company's pharmaceutical products met international regulatory requirements.
Education and Pharm D from University of Limoges
Huguette Stephanie Bodo Kamga holds a Pharm D degree from the University of Limoges, where she studied pharmacy from 1997 to 2003. This six-year educational foundation prepared her for a successful career in regulatory affairs and pharmacovigilance within the pharmaceutical industry.
Background in Regulatory Affairs and Labeling Strategy
With over 15 years of experience, Huguette Stephanie Bodo Kamga has held numerous roles within regulatory affairs and labeling strategy. She started her career at Pfizer in 2007 as a Regulatory Affairs Pharmacist. She has extensive experience in regulatory labeling, having worked at Baxter Healthcare, Eisai, Shire, and Ironwood Pharmaceuticals. Her roles have ranged from Safety Reviewer Pharmacovigilance to Manager of Regulatory Affairs Labeling, and finally to senior leadership positions.
Roles at Baxter Healthcare
Huguette Stephanie Bodo Kamga's career includes multiple positions at Baxter Healthcare. From 2009 to 2011, she worked as a Product Surveillance Associate for Medical Devices, followed by a role as Safety Reviewer in Pharmacovigilance from 2011 to 2012. She then served as a Senior Regulatory Affairs Associate (Labeling) from 2012 to 2014. These roles collectively contributed to her expertise in regulatory compliance and safety surveillance within the pharmaceutical industry.