Nancy Sperling Email & Phone Number

Independent Consultant

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Nancy Sperling Location

Hatfield, PA, US

Nancy Sperling Work

2023 -now Independent Consultant @ Nancy J Sperling Independent Consultant
2020 -2022 Senior Quality Engineer @
2018 -2019 Quality Engineer 2 and Medical and Technical Writer @
2017 -2017 Sr. Compliance Specialist in Compliance and Risk Management in Supply Chain @
2014 -2017 Senior Technical and Medical Writer @
2013 -2014 Staff Compliance Engineer in Quality and Compliance and Regulatory @
2012 -2013 QA Compliance Manager @
2011 -2012 Quality Assurance Associate Manager-GMP, Quality Management @
1992 -2010 Quality and Regulatory Compliance Manager @

Nancy Sperling Education

Temple University
MS (Quality Assurance/Regulatory Affairs)
2006-2009
St. John's University
MS (Toxicology)
Iowa State University
BS (Animal Science Pre Vet Med)

Nancy Sperling Skills

Good Manufacturing Practice (GMP), audit, change,project and risk management, regulatory, writing
Auditing, Consent Decree
CAPA, Investigations, Deviations, Change Control
Method Transfer, Compendial Affairs and Regulatory Compliance
CAPA
Change Control
GMP
GLP
21 CFR Part 11
Method Transfer
Auditing
Validation
FDA
Compliance
Sop
HPLC
Regulatory Affairs
Pharmaceutical Industry
LIMS
V&V
Technology Transfer
Regulatory Requirements
Quality Assurance
UV/Vis
Quality Auditing
Quality Control
Computer System Validation
Pharmaceutics
Six Sigma
Laboratory
Quality System
Cleaning Validation
GxP
Drug Development
Dissolution
Technical Leadership
Gas Chromatography
Medical Devices
Clinical Development
Cross-functional Team Leadership
Professional Mentoring
Quality Management
Standard Operating Procedure (SOP)
Good Laboratory Practice (GLP)
Corrective and Preventive Action (CAPA)
U.S. Food and Drug Administration (FDA)
Project, Change & Risk Management, Audit, Technical Writing,CAPA,
Project, Change & Risk Management, Audit, Technical Writing,CAPA,Food and Drug Law, Quality Audit, Good Laboratory Practice, Drug Development, Good Clinical Practices, Bioethics, Post-Approval Changes, Project Management, Advanced GMPs, Global Excipient Regulations, IND/NDA Submissions, Global Medical Device Regulations.
Project, Change & Risk Management, Technical Writing,CAPA,Food and Drug Law, Quality Audit, Good Laboratory Practice, Drug Development, Good Clinical Practices, Bioethics, Post-Approval Changes, Project Management, Advanced GMPs, Global Excipient Regulations, IND/NDA Submissions, Global Medical Device Regulations. Pharma, Medical Devices, Biological,Clinical and Consumer Health. R&D. Manufacturing, Distribution and Supply Chain.
Medical Diagnostics
Sample Management
Consulting
Specifications
Suppliers
Chemical
TLC
Printing
Corrective Actions
Chemistry
Ocd
Clinical And Consumer Health
Vendors
Sales
ISO
Supply Operations
Manages
Trend Analysis
Quality Audit
Ind/Nda Submissions
Clinical Research
Net
R&D. Manufacturing
Franchising
Oversight
Arthritis
Distribution And Supply Chain
Consent Decree
Protocol
NDA
Bioprocess
Co Authored
Deviations
Cross Functional Team Leadership
Technical Transfers
Facilitation
Legal
U.S. Food And Drug Administration Fda
Third Party
Value Stream Mapping
Direct Mail
Regulatory Compliance
Global Excipient Regulations
Dragon
CMC
Regulatory Agencies
DEA
Management
Ibm Rational Purify
Standard Operating Procedure Sop
Jamaica
Cssgb
Science
Phase 1
21Cfr
Toxicology
Auditor
Metrics
CQA
Database Administration
Data Storage
Pfizer
Clinical Practices
Monitors
Compliance Training
Good Laboratory Practice Glp
Publications
Blood
Internal Staff
Brio Query
Approvals
Database Management
Cros
Philadelphia
Reconcile
Guidance
Data Validation
Consumer
Troubleshooting
Team Leadership
Client Requirements
Template
Destruction
Strategies
Microsoft Office
Medicine
Global Medical Device Regulations
Testing
Readiness
ASQ
EDI
Training
Microsoft Excel
Fair Use
Bioethics
Policy
Trending
Web Based Reporting
Enterprise Software
Sds
Meticulous
Order Fulfillment
Batch Release
Robust
Documentation
Project Management
Product Development
American
Research
Investigation
Information Management
Call Centers
Commercial Real Estate
Raritan
Rivers
Drawing
Analysis
Animal Science
Computer System
Investigations
Pdma
See 27+See Less
Verizon
Pai
Jersey
Cross Functional Team
Western Blotting
Enzymes
Site Inspections
Heavy Metals
FIX Protocol
Tissue
Accountability
St. John
Fayette
Biological
Carbohydrate
Client Services
Schedules
Detail
Laboratory Equipment
Scientific
Operations
Osteoarthritis
Advanced Gmps
Analytical Chemistry
Risk Assessment
Maintenance
Global Drug Development
Marketing
Change Management
Documentum
Performing
Project
Remediation
Pharmacology
Supports
Data Integrity
Written Communication
Incident Investigation
Pearl
Laptops
Presentations
Batch Records
Iowa
LinkedIn
ISO 13485
Internal Audit
Policies and Procedures
Regulations
Distribution
International
CRO
Google Groups
Monographs
Food
Veterinary Medicine
Data Management
Report Writing
Teaching
Warehousing
Food And Drug Law
Compliance Oversight
Reviews
Stat
Regulatory Standards
ICH guidelines
Green Belt
Guidelines
Pharma
Global Excipient Regulati
Diagnostics
Patient Outcomes
ADP Payroll
Corrective And Preventive Action Capa
Technical Writing
Change And Risk Management
21Cfr820
CMOS
Independent Contributor
Audit
Terminology
Manufacturing
Good Clinical Practices
Internal Controls
Post Approval Changes
Protein Assays
Vaccines
Transfusion Medicine
Good Laboratory Practice
Ortho
Meetings
Supply Chain
Compendial Affairs And Regulatory Compliance
Third Party Vendors
Analytical Method Validation
Coordinated
Cglp
Standard Operating Procedure
Corrective and Preventive Action
u.s. Food and Drug Administration

Nancy Sperling Summary

Nancy Sperling, based in Hatfield, PA, US, is currently a Independent Consultant at Nancy J Sperling Independent Consultant. Nancy Sperling brings experience from previous roles at Stryker, BD, Celgene and Novartis. Nancy Sperling holds a 2006 - 2009 MS in Quality Assurance/Regulatory Affairs @ Temple University. With a robust skill set that includes Good Manufacturing Practice (GMP), audit, change,project and risk management, regulatory, writing, Auditing, Consent Decree, CAPA, Investigations, Deviations, Change Control, Method Transfer, Compendial Affairs and Regulatory Compliance, CAPA and more. Nancy Sperling has 1 emails and 1 mobile phone numbers on RocketReach.