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Himani Parikh Location
United States
Himani Parikh Work
Vice President Regulatory Affairs and Medical Writing @ (August 2025 - Present)
Executive Director Regulatory Affairs @ (June 2023 - July 2025)
Senior Director Regulatory Affairs @ (April 2022 - June 2023)
Director of Regulatory Affairs @ (April 2021 - April 2022)
Associate Director Regulatory Affairs @ (April 2020 - April 2021)
Senior Manager Regulatory Affairs @ (May 2016 - March 2020)
Co-Chair, Women Leadership Association @ (January 2018 - November 2019)
Global Regulatory Affairs Lead @ (September 2013 - May 2016)
Global Regulatory Operations, Abbott Established Pharmaceutical Division @ (September 2012 - September 2013)
Supplier Quality Specialist @ (June 2011 - December 2012)
GCP and Pharmacovigilance Compliance Specialist @ Takeda (March 2008 - August 2010)
Himani Parikh Education
Illinois Institute of Technology
Master's in Science (Molecular Biology)
The Maharaja Sayajirao University of Baroda
Post Graduate (Biochemistry)
Sardar Patel University
B.S (Biotechnology)
Himani Parikh Skills
Supplier Quality
FDA
Quality Assurance
GMP
Quality System
Pharmaceutical Industry
CRO
Molecular Biology
Pharmacovigilance
Cell
PCR
Medical Devices
CAPA
Regulatory Requirements
Validation
GxP
Clinical Research
Quality Auditing
Regulatory Affairs
Sop
Computer System Validation
Biotechnology
Change Control
Design Control
Software Documentation
Regulatory Submissions
Planning
Regulatory
Strategic Planning
Himani Parikh Summary
Himani Parikh, based in United States, is currently a Vice President Regulatory Affairs and Medical Writing at Partner Therapeutics. Himani Parikh brings experience from previous roles at Iovance Biotherapeutics, Inc., BeiGene and AbbVie. Himani Parikh holds a Master's in Science in Molecular Biology @ Illinois Institute of Technology. With a robust skill set that includes Supplier Quality, FDA, Quality Assurance, GMP, Quality System and more. Himani Parikh has 2 emails and 1 mobile phone numbers on RocketReach.
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