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 (Key Coursework: Food and Drug Law, Quality Audit, Good Laboratory Practice, Drug Development, Good Clinical Practices, Bioethics, Post-Approval Changes, Advanced GMPs, Global Excipient Regulations, IND/NDA Submissions, Global Medical Device Regulations.)
2006-2009 - St. John's University
MS (Toxicology)
-
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
- 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 Key Coursework: Food and Drug Law, Quality Audit, Good Laboratory Practice, Drug Development, Good Clinical Practices, Bioethics, Post-Approval Changes, Advanced GMPs, Global Excipient Regulations, IND/NDA Submissions, Global Medical Device Regulations. @ 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.
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