Manisha Chukkapalli, MS, possesses extensive experience in regulatory affairs and project management within the life sciences and healthcare sectors. Starting as a Residential Safety Proctor at Northeastern University, Manisha advanced to various roles, including Quality Assurance Project Coordinator at ImmunoGen, Inc., and Regulatory Project Coordinator at Charles River Laboratories. As a Senior Regulatory Affairs Operations Specialist at Cardinal Health, responsibilities included analyzing and maintaining project data and managing labeling processes. Manisha further excelled as a Product Labeling Project Coordinator at DePuy Synthes Companies, creating and revising product labeling to meet regulatory standards. Currently, Manisha serves as a Senior Regulatory Affairs Process Specialist at Cepheid, recently transitioning to Regulatory Affairs Principal Specialist, showcasing a commitment to regulatory excellence and process optimization.
Location
United States
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