Developmental Scientist @ (December 2005 - April 2007)
Quality Analyst II and III @ B. Braun Medical (May 2006 - August 2006)
ASSISTANT SCIENTIST @ RI CHEMICAL (January 2004 - January 2005)
Mayur Patel Education
Fullerton College 1999-2001
Troy High School 1999-1999
El Dorado High School 1997-1999
California State University-Dominguez Hills
Master of Science - MS (Quality Assurance (Manufacturing))
2016
UC Irvine
Medical Product Development
2009
California State University, Fullerton
Bachelor of Science - BS (Biochemistry)
2004
Mayur Patel Skills
21 CFR Part 11
Biotechnology
CAPA
Certified Quality Engineer (CQE)
Change Management
Corrective and Preventive Action (CAPA)
Design Control
Design of Experiments
FDA
GLP
GMP
Gage R&R
Good Laboratory Practice (GLP)
GxP
ISO 13485
Internal Audits
LIMS
Lead Change
Life Sciences
Lifesciences
Medical Devices
Microbiology
Process Improvement
Project Management
Quality Assurance
Quality Auditing
Quality Control
Quality Operations
Quality System
Regulatory Affairs
SOP
Six Sigma
Stability Programs
Stability Studies
Stability Testing
Standard Operating Procedure (SOP)
Team Leadership
Team Management
Total Quality Management (TQM)
U.S. Food and Drug Administration (FDA)
V&V
Validation
Verification and Validation (V&V)
Chromatography
ISO
Pharmacueticals
Wise
Discrepancy Resolution
Particle
U.S. Food And Drug Administration Fda
Design
Aseptic Processing
Photometry
GAP
PowerPoint
In Process
Good Laboratory Practice Glp
Lean Manufacturing
Cream
Drug Product
Qualification
Capas
Process Validation
Troubleshooting
System
Flat Patterning
Disinfection
Inventory
Tank
Risk Management
Documentation
Physical Chemistry
Finishing
UV
Homogenizer
Validation Master Plans
Jersey
C
Capping
Sensors
Liaison Between Departments
Communication
Active
Filtration
Uf/Df
Data Review
Surface
Pharmacy
Ultra
Responsibility
Colorimeter
Injection Molding
Regulations
Ph Meter
Obtain
cGMP manufacturing
Teaching
Defects
Guidelines
Raw Materials
Corrective And Preventive Action Capa
Technical Writing
Wet Chemistry
Compliance
Preventive Maintenance
Engineering Drawings
Microsoft Word
Challenging Environment
Organic Chemistry
Pharmaceutics
Vacuum
Plate
Disintegration
Ortho
Writing
Supplies
Sound
Printing
Chemistry
cGMP
Surfactants
Bacterial
Data Entry
Filter
Cycles
Rationale
Trackwise
White Belt
Standard Operating Procedure Sop
Checking
Punching
SharePoint
Blood
Methodology
Data Validation
Metals
Cleaning
Reports
Engineering
Conveyors
Water Distribution
Testing
Press
Barcode Scanners
Production Techniques
Supply
Trains And Add Rails
Research
System Monitoring
Precision Engineering
Investigation
Environmental Monitoring
Inspection
Written
Humidity
Solutions Marketing
CIP
Washers
Gas Chromatography
Endotoxin
Lal
Emulsions
Configurations
FIX Protocol
Data Collection
Highly Motivated Self Starter
Sheet
Remedies
OOS
Risk Assessment
Peer Reviews
Maps
Drafting
Cosmetics
Quantitative Analytics
Vitamins
SAT
Documentum
Hair Care
Colorimetry
Thinking
OSHA
Standardization
Media
Fault Tree Analysis
Qualifying
Centrifuge
Multi Tasking
Logic Gates
Materials
Outlook
Terminology
Test Procedures
Analytical Instruments
IR
Formulation
Analytical Method Validation
Evaluation
Bottling
Databases
Medical Diagnostics
Chemical
Units
Mmr
SEP IRA
APIs
Aql
Conductivity
Working Experience
Delta V
SPC
Science
Route
TOC
Integration
Analyzer
Gel
Labels
Equipment Qualification
OTC
Pharmaceutical Research
Instrumentation
Picking
Software Documentation
Process Flow
Bangalore
Tests
Method Development
Circuits
Strategy
Microsoft Office
Microsoft Excel
Trending
Glass
Technical Reports
Plasma Physics
Medicinal Chemistry
Assembly
Scheduling
Validations
Pharmaceutical Packaging
Analysis
Process Simulation
ROOT
Laboratory
Thermo
Harmonization
Verification And Validation V&V
Structural Drying
Applications
Data Analysis
Mechanical
Process Excellence
Compression
FMEA
Contemporary Art
SIP
Process Capability
Capsules
Document Management
Microsoft Project
Autoclave
Project
Coupons
Health Sciences
Spectrophotometry
Batch Records
Counters
Ancillary
Council
Packaging
Analytical Equipment
Bas
Root Cause Analysis
Warehousing
Forms
Commissioning
Dialysis
Bulk
Dissolution
India
Tablets
Nutraceuticals
Sampling
Calibration
Compressed Air
Consumer Healthcare
Acceptance Criteria
Pharmnet
Pharmacokinetics
Bmr
TLC
Process Analytical Technology
Insurance
Heat Exchangers
Water Sampling
Particle Size
Pharmaceutical Manufacturing
Change Control
Coatings
Data Mapping
Induction
Minitab
Utilities
Reagents
Batch Processing
Mixing
Fire Management
Fat
Management
General Electric
Aseptic
Materials Science
Spray
Execution
HPLC
Acceptance Testing
Cell
Data Recovery
Pharmaceutical Engineering
Information Extraction
Drug Delivery
EDI
Qualitative Research
Reporting
Locating
Raritan
Hardness
Steam
Sterilization
Concepts
Production Operations
Tanks
Lync
Laminating
GDP
Operations
Technical Support
Measurements
UV/Vis
Project Leaders
Oven
Electronics
ICH guidelines
Visio
Cleaning Validation
Software
Stain
Resolving Issues
Aptitude
Limits
Manufacturing
Blending
Summary Reports
Stability
Change Process
Decision Making
Skin
Pharmaceutical Industry
Problem Solving
Meetings
Mock
Diagrams
Piping
u.s. Food and Drug Administration
Verification and Validation
Good Laboratory Practice
Corrective and Preventive Action
Standard Operating Procedure
Certified Quality Engineer
Total Quality Management
Mayur Patel Summary
Mayur Patel, based in United States, is currently a Scientist at Naval Surface Warfare Center, Corona Division. Mayur Patel brings experience from previous roles at Advanced Sterilization Products (ASP) and Johnson & Johnson. Mayur Patel holds a 1999 - 2001 Fullerton College. With a robust skill set that includes 21 CFR Part 11, Biotechnology, CAPA, Certified Quality Engineer (CQE), Change Management and more. Mayur Patel has 4 emails and 3 mobile phone numbers on RocketReach.
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