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Dave Willis Location
California, United States
Dave Willis Work
Director Drug Product Manufacturing @ (June 2022 - Present)
Director Manufacturing Systems and Compliance @ (December 2020 - June 2022)
Interim Head Manufacturing Systems and Compliance @ (February 2020 - December 2020)
Associate Director Manufacturing Compliance @ (November 2018 - December 2020)
Associate Director Upstream Manufactuing @ (July 2015 - April 2018)
Sr. Manager Technical Services and Warehouse Operations @ (March 2014 - July 2015)
Senior Manager RIBA production and Manufacturing Improvements @ (July 2011 - March 2014)
Operations Manager @ (January 2010 - July 2011)
Senior Manager Production @ (November 2004 - August 2010)
Interim Director Packaging and Materials Management @ (January 2007 - November 2007)
Packaging Manager @ (November 2004 - November 2007)
Packaging Department Manager @ (August 2003 - November 2004)
Capital Projects Manager @ (January 1998 - January 2004)
Office Automation Specialist @ (January 1997 - January 1998)
Production Supervisor @ (March 1993 - August 1997)
Assistant Director The Continentals @ Continental Singers (June 1992 - January 1993)
Chemist @ GTEL Environmental Labs (January 1990 - January 1992)
Dave Willis Education
Grand Canyon University
Master's degree (Biology, General)
2021-2022
California Polytechnic State University
Bachelor's Degree (Biological Sciences)
1987-1990
Los Medanos College 1985-1987
California Polytechnic State University-San Luis Obispo
Bachelor of Science - BS (Botany/Plant Biology)
1990
Clayton Valley HS
Dave Willis Skills
Site Operations
Interpersonal Communication
Parenteral
Communication
Production Management
Warehouse Operations
Production Planning
Manufacturing Operations
Key Performance Indicators
Aseptic Processing
Visual Inspection
Cross-functional Team Leadership
Quality Assurance
Manufacturing
Sop
Packaging
Validation
GMP
SAP
Process Improvement
Pharmaceutical Industry
Technology Transfer
Product Development
Continuous Improvement
CAPA
Supply Chain
FDA
Medical Devices
Quality System
21 CFR Part 11
Biotechnology
Change Control
V&V
GLP
Biopharmaceuticals
Business Process Improvement
Corrective and Preventive Action (CAPA)
Good Laboratory Practice (GLP)
SAP Products
Standard Operating Procedure (SOP)
Supply Chain Management
U.S. Food and Drug Administration (FDA)
Verification and Validation (V&V)
Management
Life Sciences
Project Management
Operational Excellence
GxP
Leadership
Capital Budgeting
EBR
External Audits
IT Integration
Lean Management
Lean Process Improvement
Project Engineering
Regulatory Compliance
Technical Leadership
Research
Technical Services
Customer Service
Sales
Operations
Services
Upstream
Glassware
Strategic Planning
Cross Functional Team Leadership
Change Management
Good Laboratory Practice Glp
Verification and Validation V&V
Corrective and Preventive Action Capa
u.s. Food and Drug Administration Fda
Standard Operating Procedure Sop
Standard Operating Procedure
u.s. Food and Drug Administration
Verification and Validation
Corrective and Preventive Action
Good Laboratory Practice
Account Management
People Management
People Development
Dave Willis Summary
Dave Willis, based in California, United States, is currently a Director Drug Product Manufacturing at Boehringer Ingelheim. Dave Willis brings experience from previous roles at Boehringer Ingelheim and Grifols. Dave Willis holds a 2021 - 2022 Master's degree in Biology, General @ Grand Canyon University. With a robust skill set that includes Site Operations, Interpersonal Communication, Parenteral, Communication, Production Management and more. Dave Willis has 2 emails and 1 mobile phone numbers on RocketReach.
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