Formulation R and D Documentation Specialist @ (October 2017 - November 2019)
CMC Technical Writer @ (August 2016 - October 2017)
Regulatory Technical Writer Intern @ (April 2016 - June 2016)
Global Regulatory Affairs Specialist @ (November 2015 - April 2016)
Research Volunteer @ (January 2015 - May 2015)
Regulatory Affairs Intern @ (May 2014 - August 2014)
Manufacturing Intern @ (April 2013 - May 2013)
Maitri Mehta Education
Northeastern University
Master's Degree (Regulatory Affairs for Drugs, Biologics and Medical Devices)
2014-2016
Nirma University, Ahmedabad, Gujarat, India
Bachelor's Degree (Pharmacy)
2010-2014
Goldey-Beacom College
Maitri Mehta Skills
Microsoft Office
Regulatory Affairs
Microsoft Excel
Pharmaceutical Industry
PowerPoint
Quality Assurance
SOP
Microsoft Word
Research
Clinical Trials
HPLC
Management
Teamwork
Biotechnology
GMP
Validation
Life Sciences
Pharmaceutics
Regulatory Compliance
Public Speaking
ANDAs
NDA
Clinical Research
R&D
Biologics
Medical Devices
Regulatory Submissions
FDA
GLP
Leadership
GCP
Data Analysis
IND
U.S. Food and Drug Administration (FDA)
Standard Operating Procedure (SOP)
High-Performance Liquid Chromatography (HPLC)
Isi Writer
High Performance Liquid Chromatography Hplc
Change Control
Qumas
Isi Toolbox
U.S. Food And Drug Administration Fda
Standard Operating Procedure Sop
Standard Operating Procedure
High Performance Liquid Chromatography
u.s. Food and Drug Administration
Maitri Mehta Summary
Maitri Mehta, based in Piscataway Township, NJ, US, is currently a Regulatory Affairs Project Manager at Roche. Maitri Mehta brings experience from previous roles at Roche and Kashiv BioSciences LLC. Maitri Mehta holds a 2014 - 2016 Master's Degree in Regulatory Affairs for Drugs, Biologics and Medical Devices @ Northeastern University. With a robust skill set that includes Microsoft Office, Regulatory Affairs, Microsoft Excel, Pharmaceutical Industry, PowerPoint and more. Maitri Mehta has 2 emails and 1 mobile phone numbers on RocketReach.
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