2012 -2013 Validation Engineer Consultant for Atrium Staffing @
2011 -2012 Validation Analyst @
2010 -2010 Process Development Scientist @
2008 -2008 Production Chemist @ Medwin
Ankitkumar Patel Education
Stevens Institute of Technology
Master of Science (M.S.) (Pharmaceutical Manufacturing)
2009-2010
Rajiv Gandhi University of Health Sciences
Bachelor (Pharmaceutical Sciences)
2003-2007
Ankitkumar Patel Skills
Validation
Sop
IQ
OQ
PQ
GMP
CAPA
Document Review
Technical Writing
TLC
FMEA
Minitab
Instrument Validation
Validation Master Plans
Cleaning Validation
MS Project
Microsoft Office
Design of Experiments
GLP
GxP
swab sampling
Formulation
Calibration
Process Flow Documentation
Risk Assessment
Traceability Matrix
Change Control
Regulatory Guidelines
Bioprocess
Pharmaceutical Industry
Pharmaceutical Packaging
CIP
SIP
Pharmacokinetics
Pharmaceutics
Quality Assurance
V&V
Regulatory Affairs
Good Laboratory Practice (GLP)
CSV
Cip Systems
Pharmaceutical Manufacturing
Biotechnology
Product Analysis
Coatings
Data Mapping
Utilities
Reagents
Pharm
Deviations
Temporary Placement
Cross Functional Team Leadership
Assessment
Fat
Pilgrim
Serialization
Management
Design
Reality
Standard Operating Procedure Sop
Science
Physiology
Technical Operations
Statistics
21 CFR Part 11
System Requirements
21 CFR
In Process
Good Laboratory Practice Glp
Lean Manufacturing
SharePoint
Execution
Equipment Qualification
Qualification
Process Validation
Engineering Economics
System
Team Management
Process Flow
Tests
Pharmaceutical Engineering
Engineering
Reports
Strategy
Verifying
Human Anatomy
Process Control
Testing
GCP
ASQ
Training
Artifacts
Gage R&r
Medicinal Chemistry
Documentation
Project Management
Informatics
Quality Control
American
Research
Process Engineering
Precision Engineering
LIMS
Investigation
Microsoft
R&d
Analysis
Process Simulation
Hardness
Project Charter
Finishing
SAP
Test Planning
Instrumental
Computer System Validation
Product Transfer
GAMP
FIX Protocol
Ispe
Schedules
Contemporary Art
Compression
ERP
Design Specifications
Quality by Design
Author
Weight
Research and Development R&d
Process Capability
Microsoft Project
Stability Testing
SAT
Project
Data Review
Health Sciences
Pharmacy
Encapsulation
Biochemistry
Data Integrity
White Collar Criminal Defense
Technology Transfer
Batch Records
Responsibility
Internal Audit
Process Equipment
Rtm
Usa
Packaging
Regulations
International
Root Cause Analysis
Pharmaceutical Microbiology
Purified Water
Commissioning
Reviews
HVAC
Electronics
Green Belt
Environmental Remediation
Process Improvement
Visio
Raw Materials
Software
Compliance
Granulation
Requirement Specifications
Test Scripts
Organic Chemistry
India
Manufacturing
Internal Controls
Blending
Turing
Tablets
Inorganic Chemistry
Sampling
Optimization
Risk
Cost Benefit
Problem Solving
Summarize
Retirement
FDA
Process Optimization
Process Improvement Projects
Research and Development
Standard Operating Procedure
Good Laboratory Practice
Ankitkumar Patel Summary
Ankitkumar Patel, based in Cherry Hill, NJ, US, is currently a Validation Manager at Hikma Pharmaceuticals. Ankitkumar Patel brings experience from previous roles at Hikma Pharmaceuticals and West-Ward Pharmaceuticals. Ankitkumar Patel holds a 2009 - 2010 Master of Science (M.S.) in Pharmaceutical Manufacturing @ Stevens Institute of Technology. With a robust skill set that includes Validation, Sop, IQ, OQ, PQ and more. Ankitkumar Patel has 3 emails and 1 mobile phone numbers on RocketReach.
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