Darryl Prater Email & Phone Number

Sr. QA Engineer CSV and Data Integrity @ INCOG BioPharma Services

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Darryl Prater Location

Indianapolis, IN, US

Darryl Prater Work

2026 -now Sr. QA Engineer CSV and Data Integrity @
2025 -2025 Sr. Specialist, Quality Analytical Services @
2023 -2024 QA Lead Specialist - Validation and Engineering @
2013 -2023 App Technical Support Assoc Manager @
2013 -2023 Validation, Sr. Specialist @
1999 -2023 Committee on Chemical Safety @
2012 -2013 IT CSV Analyst @
2011 -2012 Quality System Consultant @ Validant @
2010 -2011 Quality Assurance Specialist @ REGISTRAT MAPI
2003 -2010 Sr IT Analyst - Mfg @ Eli Lilly & Company
2003 -2010 Analytical Validation Coordinator @ Eli Lilly & Company
2003 -2010 Sr. IT Analyst and Validation Coordinator @ Eli Lilly & Company
2003 -2010 Senior Validation Engineer @ Eli Lilly & Company
2000 -2003 Instrument and Computer Specialist @
2000 -2003 Instrument and Computer Specialist @
1996 -2003 Metrology Liaison @

Darryl Prater Education

Fisk University
B. S. (Yearbook Staff, Photography, WFSK Radio Station)
1983-1987
Fisk University
Bachelor of Science (BS) (BS Chemistry)
1983-1987
Citronelle High School
High School (Advanced AP courses Yearbook staff, Student Government, Who's Who Among American )
1979-1983

Darryl Prater Skills

Validation
FDA
GMP
21 CFR Part 11
Quality Assurance
Quality System
LIMS
Computer System Validation
HPLC
Quality Control
Training
Testing
Software Documentation
Chemistry
Change Control
Gas Chromatography
SOP
CAPA
GLP
UV/Vis
Medical Devices
Biopharmaceuticals
GxP
GAMP
Databases
Document Management
SDLC
Auditing
Change Management
ISO
Risk Assessment
FDA GMP
Compliance
Business Analysis
Business Process
Software Quality Assurance
Requirements Analysis
EMEA
Laboratory Informatics
cGMP practices
Supplier Management
Computer Security
Data Integrity
Requirements Traceability
Laboratory Automation
Data Protection Manager
Security Audits
Software Development Life Cycle (SDLC)
U.S. Food and Drug Administration (FDA)
Laboratory Information Management System (LIMS)
Chromatography
Traceability Matrix
Clinical Trials
Consulting
Readers
Chemical
Corrective Actions
Vendors
Community
Phase Ii
On Site
Pharmaceutical Manufacturing
Customer Oriented
Clinical Research
Agile Methodologies
Geometric Dimensioning And Tolerancing
Trackwise
Functional Specifications
Oversight
FTIR
Qas
SOP authoring
Construction
Mapi
Application Lifecycle
SME
Clinical Development
Mass Spectrometry
Batch Processing
Software Quality
Keil
U.S. Food And Drug Administration Fda
Assessment
Travel
Validation Reports
Regulatory Agencies
Management
Toastmasters
Design
Cyber
Contractors
Assurance
Corporate Actions
Resume
NIR spectroscopy
Beckman
Integration
Lubricants
Pfizer
Monitors
21 CFR
Affiliation
Human Resources
Qualification
Profit
Guidance
Instrumentation
Process Validation
System
Business Services
Atlanta
Healthcare
Photography
Contract Work
Piloting
Risk Management
GCP
Policy
Computerized Systems
External Clients
Documentation
Scheduling
American
Research
Earlier
Emerging Technologies
Reporting
Empower
Application Lifecycle Management
R&D
Philips
Analysis
Trails
Inspection
Written
Computer System
Advertising Agency
Music Appreciation
Customer Negotiations
Laboratory
Gap Analysis
Broad Based
Thermo
R
SAP
Requirements
Test Planning
Experimentation
Gas
Yahoo
Personal Data Protection
Process R&D
Coordination
FIX Protocol
Fuel
Applications
Specs
It Liaison
ERP
User Requirements
Safety
Operations
Data Security
Surprise
Perkin Elmer
Laboratory Information Management System Lims
Project Planning
GC/MS
Remediation
External Audit
Project
Contractual Agreements
House
Supports
Data Protection Act
Losses
Software Development Life Cycle Sdlc
Additives
Responsibility
Internal Audit
Regulations
Security Risk
International
CRO
Analytical Equipment
History
Curriculum Design
Electronics
Letters of Credit
ICH guidelines
Discovering
Bridge Inspection
Software
E Learning
Technical Writing
Dissolution
Agilent
Test Scripts
Pharmaceutics
Manufacturing
Legacy Systems
Plate
Optimization
Risk
Metrology
Multi Site
Large Projects
Automation
u.s. Food and Drug Administration
Laboratory Information Management System
Software Development Life Cycle

Darryl Prater Summary

Darryl Prater, based in Indianapolis, IN, US, is currently a Sr. QA Engineer CSV and Data Integrity at INCOG BioPharma Services. Darryl Prater brings experience from previous roles at Hikma Pharmaceuticals, Catalent Pharma Solutions and Accenture. Darryl Prater holds a 1983 - 1987 B. S. in Yearbook Staff, Photography, WFSK Radio Station @ Fisk University. With a robust skill set that includes Validation, FDA, GMP, 21 CFR Part 11, Quality Assurance and more. Darryl Prater has 3 emails and 2 mobile phone numbers on RocketReach.