2015 -
2015 Quality Assurance Manager, site lead @
2013 -
2015 Senior Quality Assurance Specialist, site lead @
2013 -
2013 Qa Supervisor @
2010 -
2013 QA Associate @
2009 -
2009 QA Validation ( co-op) @
Ruchit Doshi Education
Stevens Institute of Technology 2008
-
2010
KLE college of pharmacy 2003
-
2007
Ruchit Doshi Skills
FDA
Validation
Sop
Batch Records
Quality Assurance
CAPA
Annual Product Review
FDA GMP
Cleaning Validation
Change Control
Pharmaceutics
Deviations
Quality Auditing
OOS
cGMP practices
SPC
Equipment Qualification
Pharmaceutical Industry
Protocol
Calibration
GMP
GxP
21 CFR Part 11
LIMS
ANDA
GLP
UV/Vis
U.S. Food and Drug Administration (FDA)
Standard Operating Procedure (SOP)
Abbreviated New Drug Application (ANDA)
U.S. Title 21 CFR Part 11 Regulation
Corrective and Preventive Action (CAPA)
Good Laboratory Practice (GLP)
Good Laboratory Practice Glp
Safety Management Systems
Abbreviated New Drug Application Anda
Process Improvement
Corrective And Preventive Action Capa
Customer Service
U.S. Food And Drug Administration Fda
Management
Standard Operating Procedure Sop
Writing
Chromatography
Chemical
Process Analytical Technology
Pharmaceutical Manufacturing
Clinical Research
Biotechnology
Regulatory Affairs
Digital Preservation
Coatings
Data Mapping
Minitab
Australia
Bioprocess
Batch Processing
Bench
Design of Experiments
Japan
Travel
DEA
Design
Academic Publishing
Science
TOC
Auditing
Circulation
Public Speaking
Qualification
HPLC
Seminars
Process Validation
Manuals
System
Cell
Education
Copies
Bangalore
Osd
Pharmaceutical Engineering
Cleaning
Reports
Engineering
Titration
Microsoft Office
Materials Testing
Microsoft Excel
Testing
Chips
Product Reviews
Training
Trending
Root Cause
Deviation Management
Documentation
Project Management
Informatics
Quality Control
Research
Reporting
Investigation
EMA
Downstream Oil and Gas
Building Design
Environmental Monitoring
Analysis
Written
Process Simulation
Finishing
Concepts
Intellectual
Sports
Coordination
Upstream
FIX Protocol
Elocution
Ispe
Communication
Contemporary Art
Music
Chocolate
Quality System
Microsoft Project
Spec
Distribution Center Operations
House
Facilities Management
Pharmacy
Representation
Catalyst
Laptops
OSHA
Internal Audit
Six Sigma
Packaging
Regulations
Spectroscopy
International
Purified Water
Teaching
Forms
Report Compilation
Reviews
ICH guidelines
Statgraphics
Visio
Medical Devices
Software
Raw Materials
Wet Chemistry
Compliance
Satellite
Granulation
Subjects
India
Manufacturing
Internal Controls
Stability
Tablets
Sampling
Disintegration
Filing
TOEFL
Databases
Standard Operating Procedure
u.s. Food and Drug Administration
Corrective and Preventive Action
Good Laboratory Practice
Abbreviated New Drug Application
Ruchit Doshi Summary
Ruchit Doshi, based in Boston, MA, US, is currently a Senior Director, GMP Quality Assurance, Commercial at Syndax Pharmaceuticals. Ruchit Doshi brings experience from previous roles at Karyopharm Therapeutics Inc.. Ruchit Doshi holds a 2008 - 2010 Stevens Institute of Technology. With a robust skill set that includes FDA, Validation, Sop, Batch Records, Quality Assurance and more. Ruchit Doshi has 2 emails and 1 mobile phone numbers on RocketReach.
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