Dawn Benson Email & Phone Number

SVP, Quality and Product Manufacturing @ CytomX Therapeutics

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Dawn Benson Location

South San Francisco, CA, US

Dawn Benson Work

2023 -now SVP, Quality and Product Manufacturing @
2022 -2023 VP, Head of Quality @
2022 -now Vice President, Head of Quality @
2021 -2022 Senior Vice President, Head of Quality @
2021 -2022 Senior Vice President, Quality Assurance, Validation and Combination Product @
2015 -2021 Vice President, Quality Systems, Validation and Medical Devices @
2011 -2015 Senior Director, Quality Assurance and Regulatory Operations @
2011 -2011 Senior Compliance Consultant @
2008 -2011 Director, Quality Assurance and Quality Control @
2007 -2008 Senior Manager, Quality Sciences @
2006 -2007 Quality Assurance Manager, Contract Manufacturing @ Vaxgen
2003 -2006 Quality Assurance Manager @

Dawn Benson Education

University of North Carolina Wilmington
Bachelors (Chemistry)
1992-1997
University of North Carolina - Wilmington
Bachelor of Arts
1997
University of North Carolina
Bachelor of Arts
1996

Dawn Benson Skills

Quality Control
Quality Assurance
CAPA
GMP
Validation
FDA
GLP
Biotechnology
Sop
Medical Devices
Technology Transfer
Pharmaceutical Industry
Lifesciences
Biopharmaceuticals
HPLC
21 CFR Part 11
V&V
GxP
Change Control
Computer System Validation
Vaccines
Aseptic Processing
Analytical Chemistry
LIMS
IND
Regulatory Affairs
Quality System
Life Sciences
Quality Management
Good Laboratory Practice (GLP)
U.S. Food and Drug Administration (FDA)
Corrective and Preventive Action (CAPA)
Laboratory Information Management System (LIMS)
U.S. Title 21 CFR Part 11 Regulation
Standard Operating Procedure (SOP)
Writing
Substance
Clinical Trials
Suppliers
Chemical
Corrective Actions
Cell Biology
Method Transfer
Adobe Contribute
Chemistry
Significant Accomplishments
Vendors
Bacterial
Supply Operations
Concentrations
Consideration
Clinical Research
Incident Management
Oversight
SAN
Aol
Utilities
Corporate Training
Work Ethic
Contract Manufacturing
Construction
Tracking Systems
Quality Auditing
Deviations
Batch Processing
Technical Transfers
Desarrollo De Software a Medida
Non Conforming
Pda
u.s. Food and Drug Administration Fda
Regulatory Compliance
Travel
Florida
Procurement
CMC
Technical Drawing
Regulatory Agencies
Management
Standard Operating Procedure Sop
Contractors
Resume
Aseptic
Auditing
Clinical Practices
PowerPoint
Monitors
Good Laboratory Practice Glp
Ethics
Public Speaking
Lean Manufacturing
Parenteral
Human Resources
Drug Product
Qualification
Site Visits
Guidance
Job Search
Capas
Record of Success
Instrumentation
Manufacturing Operations
Troubleshooting
System
Cell
Education
MRB
Engineering
Reports
Level Iii
Supervision
Microsoft Office
Revision
Drug Delivery
Diligent
Oncology
Microsoft Excel
Testing
Intermediates
Approval Process
GCP
Training
Policy
Critical Systems
Root Cause
GCPs
Plasma Physics
Regulatory Submissions
Scheduling
Documentation
Product Development
Protein Purification
System Monitoring
Commercial Real Estate
Investigation
Information Management
Manufacturing Processes
Building Design
Analysis
Partnerships
Advertising Agency
Laboratory
R
SAP
Pai
Kind
Coordination
FIX Protocol
Ncmr
Applications
Palo Alto
Interfacing
Analytical Techniques
Ispe
Assay Development
Mechanical
Detail
Negotiation
Evidence
Business Alignment
Obsolete
Method Transfers
European Union
Proficiency Testing
Internal Compliance
Safety
Licensing
Operations
Quality by Design
Degrees
Repository
Laboratory Information Management System Lims
EDRMS
Drafting
Document Management
Timelines
Electricity
Contractual Agreements
House
CLIA
Facilities Management
Training Programs
CMO
Ctl
Services
Material Review Board
Batch Records
Suitability
Websites
Responsibility
Internal Audit
Routine Maintenance
Regulations
Qualifying
International
CRO
Biology
History
Commissioning
Reviews
Electronics
ICH guidelines
Fractionation
Guidelines
Bridge Inspection
Materials
Raw Materials
Corrective and Preventive Action Capa
Bulk
Compliance
Fermentation
San Francisco
Microsoft Word
Accompaniment
CMOS
Pharmaceutics
Manufacturing
Internal Controls
Stability
Incorporation
Job Safety
Biologics
Pre Approval
Jazz
EMEA
Large Scale Projects
Coordinate
Cglp
Commitment to Quality
Databases
Verification And Validation V&V
Good Laboratory Practice
u.s. Food and Drug Administration
Corrective and Preventive Action
Laboratory Information Management System
Standard Operating Procedure
Verification and Validation

Dawn Benson Summary

Dawn Benson, based in South San Francisco, CA, US, is currently a SVP, Quality and Product Manufacturing at CytomX Therapeutics. Dawn Benson brings experience from previous roles at CytomX Therapeutics, Cytomx Therapeutics and Coherus Biosciences. Dawn Benson holds a 1992 - 1997 Bachelors in Chemistry @ University of North Carolina Wilmington. With a robust skill set that includes Quality Control, Quality Assurance, CAPA, GMP, Validation and more. Dawn Benson has 2 emails and 2 mobile phone numbers on RocketReach.