Validation and Quality and Engineering and Facilities Consultant @ (January 2006 - October 2013)
Quality Systems Manager @ (July 2008 - July 2012)
Validation Manager @ (July 2008 - Present)
Validation Consultant @ (January 2008 - January 2008)
Validation Consultant @ (January 2005 - January 2007)
Validation Consultant @ The Macroflux Corporation (January 2006 - January 2006)
Validation Manager @ (January 2002 - Present)
Senior Validation Engineer @ Alza a Johnson and Johnson Company (January 2000 - January 2002)
Validation Specialist @ (January 1998 - January 2000)
Validation and Engineering Consultant @
David Dale Education
University Of California - Santa Barbara
Bachelor Of Science
1991-1995
David Dale Skills
Validation
GMP
FDA
CAPA
Quality System
Change Control
21 CFR Part 11
V&V
ISO 13485
Sop
Computer System Validation
GLP
Biotechnology
Medical Devices
Pharmaceutical Industry
Technology Transfer
Biopharmaceuticals
GxP
Aseptic Processing
Quality Assurance
Process Simulation
Project Management
Cleaning Validation
Lifesciences
Clinical Trials
GAMP
GCP
Chromatography
Design Control
Drug Development
Regulatory Affairs
HPLC
LIMS
Regulatory Requirements
CRO
Quality Auditing
Clinical Development
Bocce Ball
Standard Operating Procedure (SOP)
Good Laboratory Practice (GLP)
U.S. Food and Drug Administration (FDA)
U.S. Title 21 CFR Part 11 Regulation
Laboratory Information Management System (LIMS)
Corrective and Preventive Action (CAPA)
Verification and Validation (V&V)
David Dale Summary
David Dale, based in Solana Beach, CA, US, is currently a Director, GMP Compliance at Halcyon Solutions. David Dale brings experience from previous roles at Allele Biotechnology & Pharmaceuticals Inc., Sangart, Johnson & Johnson and Dexcom. David Dale holds a 1991 - 1995 Bachelor Of Science @ University Of California - Santa Barbara. With a robust skill set that includes Validation, GMP, FDA, CAPA, Quality System and more. David Dale has 3 emails and 4 mobile phone numbers on RocketReach.
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