Faaiza H.
About Faaiza H.
Faaiza H. is a Manager in CMC TW Regulatory Affairs at Bristol Myers Squibb, with extensive experience in regulatory submissions and project management across various roles and companies.
Company
Faaiza H. is currently employed at Bristol Myers Squibb, a global biopharmaceutical company. She holds the position of Manager, CMC TW, Regulatory Affairs and operates out of both Devens, MA and New Brunswick, NJ.
Title
Currently, Faaiza H. is the Manager, CMC TW, Regulatory Affairs at Bristol Myers Squibb, where she is involved in regulatory affairs submissions and strategy meetings.
Education and Expertise
Faaiza H. earned a Master of Science (MS) from Harvard University between 2019 and 2023. Prior to that, she completed her Bachelor of Science (BS) at Framingham State University. Her expertise includes proficiency with applications such as Liquent, CARA, Spotfire, and SharePoint, and she has substantial experience in Module 2 and Module 3 of regulatory affairs submissions.
Background
Faaiza H. has a robust background in the field of regulatory affairs and biopharmaceutical research. Before her current role, she served as a Senior Scientist and Associate Research Scientist at Bristol Myers Squibb, accumulating notable experience over several years. Additionally, she has held various positions at companies such as AbbVie, AmericanBio Analytical, and Framingham State University, steadily enhancing her expertise in biologics and small molecules.
Achievements
Faaiza H. has led the authoring and review of CMC Regulatory Affairs submissions to Global Health Authorities in the US, Canada, EU, and various international markets. She has managed major market filings, amendments, and health queries for both commercial and clinical markets. With considerable experience in authoring sections of regulatory applications, she has also participated in and led CMC-focused strategy meetings, collaborating with matrix teams on various regulatory documents.