Head of Global Quality Systems and Compliance @ (July 2019 - June 2021)
Associate Director, Quality Validation @ (March 2016 - June 2019)
Validation Manager @ (June 2013 - March 2016)
Validation Supervisor @ NantPharma (November 2010 - May 2013)
Project Engineer- I Validation @ (October 2009 - November 2010)
Project Engineer @ (March 2008 - October 2009)
Co-op and Intern @ (May 2007 - December 2007)
Research Assistant @ (February 2006 - May 2007)
Pharmaceutical Engineer @ (January 2003 - January 2005)
Dilip A. Education
Cleveland State University
MS (Chemical Engineering)
2006-2008
Jawaharlal Nehru Technological University
Bachelors (Chemical Engineering)
1999-2003
St.Meeras
High School
1992-1997
Dilip A. Skills
Six Sigma
Quality Management
Protocol Writing
Electronic Signatures
Sterilization
Control Charts
Pilot Plant
Computer System Validation
Root Cause Analysis
cGMP
GAMP
GMP
Chemical Engineering
GxP
Process Validation
Equipment Installation
Commissioning
Ispe
Change Control
FMEA
Validation
Cleaning Validation
Quality Assurance
Sop
Technical Writing
P&ID
Minitab
Quality System
Risk Assessment
V&V
Process Capability
Pharmaceuticals
Design of Experiments
Gage R&r
Equipment Specification
SPC
Pharmaceutical Industry
Technology Transfer
Aseptic Processing
Continuous Improvement
GLP
LIMS
ANOVA
CAPA
DMAIC
Hypothesis Testing
Computer System
Quality Systems
FDA
21 CFR Part 11
Software Validation
Dilip A. Summary
Dilip A., based in Redwood City, CA, US, is currently a Executive Director, GMP QA at Revolution Medicines. Dilip A. brings experience from previous roles at Bionova Scientific and Boehringer Ingelheim. Dilip A. holds a 2006 - 2008 MS in Chemical Engineering @ Cleveland State University. With a robust skill set that includes Six Sigma, Quality Management, Protocol Writing, Electronic Signatures, Sterilization and more. Dilip A. has 1 emails and 1 mobile phone numbers on RocketReach.
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