Regulatory Assistant @ (September 2017 - November 2017)
Regulatory Affairs Specialist II @ (September 2021 - March 2023)
Regulatory Affairs Specialist @ (March 2019 - January 2020)
Bansari Doshi Education
Northeastern University
Master of Science (M.S.) (Project Management)
2016-2018
Nirma University
Bachelor of Pharmacy (BPharm)
2012-2016
Bansari Doshi Skills
Regulatory Affairs
Project Management
Quality Assurance
U.S. Food and Drug Administration (FDA)
Claims Management
Regulatory Compliance
Literature Reviews
Clinical Data Management
Total Quality Management (TQM)
Lean Six Sigma
Medical Devices
Standard Operating Procedure (SOP)
Good Manufacturing Practice (GMP)
Corrective and Preventive Action (CAPA)
Clinical Trials
Pharmaceutical Industry
Drug Development
Good Clinical Practice (GCP)
Document Management
Risk Management
Scheduling
Cost Management
Agile Project Management
Six Sigma
Microsoft Office
Visio
Microsoft Project
Oracle Database
Leadership
Teamwork
Communication
Clinical Operations
Oracle Agile PLM
Quality System Regulations (QSR)
CE Mark
European Union Compliance
Medical Device Directive
Medical Device Reporting
Quality Assurance Processes
Project Scope Development
Electronic Common Technical Document (eCTD)
21 CFR
New Drug Application (NDA)
BLA
Premarket Approval (PMA)
510 (k)
Lean Tools
Bansari Doshi Summary
Bansari Doshi, based in United States, is currently a Regulatory Affairs Specialist III at Cepheid. Bansari Doshi brings experience from previous roles at Medtronic, Hologic, Inc., Curemark, LLC and Cepheid. Bansari Doshi holds a 2016 - 2018 Master of Science (M.S.) in Project Management @ Northeastern University. With a robust skill set that includes Regulatory Affairs, Project Management, Quality Assurance, U.S. Food and Drug Administration (FDA), Claims Management and more. Bansari Doshi has 3 emails and 2 mobile phone numbers on RocketReach.
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