Robert Dillard Email & Phone Number

Program Manager and Consultant @ Johnson & Johnson

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Robert Dillard Location

Lansdale, PA, US

Robert Dillard Work

2019 -now Program Manager and Consultant @
2016 -now Sr. Project Manager (Transformation Lead) Cranio Maxillofacial Biomaterials @
2016 -2016 Associate Director, North America Site Head Quality Assurance @
2015 -2015 Consultant, Quality and Compliance Specialist Senior, Product Quality Management @
2014 -2015 Consultant, Quality Project Manager, Quality Assurance and Regulatory Compliance @
2011 -2014 Consultant, Compliance Recall Project Specialist, Quality Assurance and Regulatory Compliance @
2008 -2011 Managing Director @ Higher Standard Engineering Consulting Services
2007 -2008 Executive Officer @ The Dillard Group
2004 -2008 2008 Graduate P.C. Rossin College of Engineering and Applied Science @
2002 -2007 Manufacturing Management @

Robert Dillard Education

University of the Sciences in Philadelphia
(Cell & Molecular Biology (Biotechnology))
2009-2012
Lehigh University
M.S. (Engineering)
2006-2008
Philadelphia University
MBA (Business Administration)
1997-1999
University of Pennsylvania
Doctoral Candidate DMD Program (School of Dental Medicine Dentistry)
1993-1995
Philadelphia College of Textiles and Sciences
Bachelor's degree (Chemistry / Business)
1987-1991

Robert Dillard Skills

Quality Assurance
Product Development
Project Management
FDA
TQM
Process Improvement
Business Process
Six Sigma
Manufacturing
Validation
Strategy
GMP
Lean Manufacturing
Supply Chain
Business Process Improvement
Continuous Improvement
Contract Management
Analysis
Operations Management
Supply Chain Management
Change Management
Leadership
Procurement
Medical Devices
Quality System
Training
Cross-functional Team Leadership
Management
Pharmaceutical Industry
Biotechnology
SOP
CAPA
Technology Transfer
R&D
Quality Control
Change Control
21 CFR Part 11
Operational Excellence
Life Sciences
Regulatory Affairs
Strategic Planning
Biopharmaceuticals
Quality Auditing
Clinical Trials
Drug Development
Corrective and Preventive Action (CAPA)
Public Speaking
Healthcare
Corrective And Preventive Action Capa
Cross Functional Team Leadership
U.S. Food And Drug Administration Fda
Hospitals
Quality Management
Recalls
Delaware
Scanning Electron Microscopy
ISO
Community
Cost
Commercialization
Clinical Research
Instruction
Mentoring
Redesigning
Staining
Complaints
Mass Spectrometry
Microbiology
Design
Aseptic Processing
Stabilization
Work Processes
Initiation
Aid
Human Resources
Qualification
Capas
Process Validation
Sun Microsystems
System
Inventory
Mass
Strategies
Medical Surgical
Medicine
Risk Management
Policy
Documentation
PMP
Commercial Real Estate
Chicago
Hardware
UV
Hostile Environments
C
Logistics
Communication
Scientific
Safety
Purification
Molecular Biology
Filtration
Statutes
Project Implementation
Indicators
Facilities Management
Pharmacy
Writes
Biochemistry
Closures
Hyper
Responsibility
Regulations
International
Obtain
Usability Testing
Manufacturing Systems
Diagnostics
Raw Materials
Racing
Robustness
Compliance
Mounting
Launches
Pharmaceutics
SEM
Risk
Writing
Supplies
Process Review
Chemistry
Clinical Pathology
Finance
Access Control
Trackwise
Consent Decree
Right First Time
Value Stream Mapping
Police
Regulatory Compliance
Canadian
Hitachi
Organizational Leadership
GLP
Metrics
Auditing
SharePoint
Workflow
Approvals
Quality Circle
Guidance
Networking
Forecasting
Customer Satisfaction
Manufacturing Operations
Cleaning
Reports
Engineering
Organizational Compliance
Change Impact Analysis
Testing
GCP
ASQ
Operational Readiness
Supply
Research
Investigation
Inspection
Written
Advertising Agency
Systems Analysis
Notification
Contingency Planning
Pai
Gas Chromatography
Computer System Validation
Management System
GAMP
Business Expansion
Business Alignment
DNA
Advertising
Container
Risk Assessment
Zero Defects
Distribution Center Operations
CLIA
Certified Lean
Title V
Golang
Metric
Dashboard
Analytics
OSHA
Presentations
Pqm
Curriculum Design
Sourcing
Inspired
Regulatory Standards
Materials
PMI
Dot Blot
Internal Controls
IR
Optimization
Mergers and Acquisitions
Evaluation
Process Optimization
Databases
Suppliers
Chemical
Vendors
Net
Manages
Flawless Execution
Incident Management
Executive Positions
Contract Manufacturing
Clearances
Organizational Structure
Closure
Real Estate Transactions
Science
Resume
Identifies
Key Performance Indicators
Integration
Committees
Clinical Pharmacy
Hard Drives
Pennsylvania
Equipment Qualification
Philadelphia
Instrumentation
Escalation
Hygiene
Trace
Supervision
Fluorescence
Microsoft Office
Closeouts
Trending
Status Reports
Surveying
American
Manufacturing Processes
High Performance Computing
Process Simulation
Laboratory
Gap Analysis
Business Review
Operational Requirements
Complaint Management
Applications
Accountability
HIPAA
Analytical Techniques
Laboratory Safety
Licensure
Regulatory Requirements
Quality by Design
Empowerment
Black Belt
Project
Streets
Contractual Agreements
Stream Processing
Internal Audit
Packaging
Labor Issues
Gel Electrophoresis
Warehousing
Reviews
Bridge Inspection
Bulk
Concerts
Extend
Financial Analysis
Regulatory Filing
Calibration
Delivery
Consumer Healthcare
Dash
Product Quality
Consulting
CSV
Corrective Actions
Remedial
Pharmaceutical Manufacturing
Consideration
APICS
Investigative Research
Aol
Url
Liquids
Batch Processing
Assessment
Process Technology
DEA
Evening
Shop Floor
Work Groups
Statistics
Aseptic
Gem
Information Systems
Monitors
Parenteral
Execution
HPLC
Cell
Business Services
Cho
Combination Products
Defect
Microscopic
Sold
Revision
Product Reviews
Forensic Analysis
Vis
Point of Contact
Product Acquisitions
Root Cause
Informatics
Reporting
Industrial Hygiene
Quality Assurance Professionals
Sterilization
Academic Institutions
Manage Budgets
Segments
Upstream
Schedules
Evidence
Digital Imaging
Operations
Degrees
Checks
Technical Support
House
Supports
Distribution
Clarification
ELISA
Environmental Engineering
Electronics
Government
ICH guidelines
Injury
Cold Chain
Cleaning Validation
Summary Reports
Stability
Decision Making
Directives
Tracks
Inclusion
Problem Solving
Meetings
EMEA
Consumer
Coordinate
u.s. Food and Drug Administration
Corrective and Preventive Action

Robert Dillard Summary

Robert Dillard, based in Lansdale, PA, US, is currently a Program Manager and Consultant at Johnson & Johnson. Robert Dillard brings experience from previous roles at DePuy Synthes Division of Johnson & Johnson, SUN PHARMA, Shire Pharmaceuticals Company, LLC and McNeil Consumer Pharmaceuticals, Johnson & Johnson. Robert Dillard holds a 2009 - 2012 University of the Sciences in Philadelphia. With a robust skill set that includes Quality Assurance, Product Development, Project Management, FDA, TQM and more. Robert Dillard has 4 emails and 2 mobile phone numbers on RocketReach.