Lewis Blair is a high-skilled expert, who works in Kite Pharma, Inc main office of which is in 116. as a Quality Assurance - Disposition since 2019. Lewis Blair has earned professional experience in more than 17 positions at various companies. Lewis Blair went to the University of Hartford and got education there. Los Angeles, California is the area, where the professional was lastly known to be living. Their phone and email can be easily accessed through SoftwareOfficial by request.
Name variants:
Lew Blair,
Lewie Blair
Last updated Jun 02, 2024
Contact Information
Workplace
Colleagues
Work History
Quality Assurance - Disposition
2400 Broadway, Santa Monica, CA 90404
from May 2019
Program Manager
Program Manager at DUSA Pharmaceuticals, a SUN Company
Jul 2017 — Nov 2017
Senior Quality Assurance Consultant
9965 Federal Dr, Colorado Springs, CO 80921
Mar 2017 — Jul 2017
Qa Consultant
100 Fordham Rd, Wilmington, MA 01887
Standardization of all Quality Management Systems across 31 sites.
Oct 2016 — Mar 2017
Qa Consultant
128 Sidney St, Cambridge, MA 02139
Batch Record Review and Release
Apr 2016 — Sep 2016
Senior Qa Manager and Consultant
420 Saw Ml, Ardsley, NY
Quality Assurance activities as part of the Quality GMP Unit
Oct 1, 2014 — Jan 1, 2015
Senior Quality Assurance Consultant
9000 Keystone Xing SUITE 230, Indianapolis, IN 46240
Mar 1, 2013 — Aug 1, 2014
Director of Quality Assurance
Monitoring and oversight of all Quality Assurance requirements within manufacturing and Quality Systems for compliance to GMP, FDA, and company guidelines
Maintain a state of readiness for...
Jan 2012 — Nov 2012
Documentation and Investigation Manager
50 Binney St, Cambridge, MA 02142
Create, review, and manage investigations during Consent Decree
Review batch records for cGMP compliance
2011 — 2011
Quality Systems
50 Northern Ave, Boston, MA 02210
QA MANAGER of Quality Systems (2008
2011)
SR. QUALITY ASSURANCE SPECIALIST (2007
2008)
CMC DOCUMENTATION MANAGER (2005
2007)
2005 — 2011
Documentation Control Manager
The Mountain Rd, Framingham, MA 01701
Direct Supervision of nine Configuration Analysts (CA) - Documentation Coordinators.
Process changes increasing productivity from 180 to 250 ECNs per month
Dramatically improved transpare...
2003 — 2005
Documentation and Quality
QUALITY ASSURANCE DOCUMENTATION MANAGER (2000 – 2003)
PROJECT MANAGER (1999 – 2003)
ENGINEERING ADMINISTRATOR / QUALITY ASSURANCE (1996 – 2003)
1996 — 2003
Education
Occupations
IT Professional
Software Tester
Scientist
Biotechnology Professional
Computer Specialist
Biologist
Biological Scientist
Skills
Quality System
Quality Assurance
Fda
Gmp
Pharmaceutical Industry
Capa
Quality Control
Medical Devices
Quality Management
Validation
Glp
21 Cfr Part 11
Change Control
Biotechnology
Software Documentation
Process Simulation
Computer System Validation
Gxp
Process Improvement
Quality Auditing
Biopharmaceuticals
Iso 13485
V&V
Regulatory Submissions
Regulatory Affairs
Cross Functional Team Leadership
Gcp
Iso 14971
Clinical Development
Design Control
Technology Transfer
Clinical Trials
Manufacturing
Sop
Aseptic Processing
Sdlc
Lims
Gamp
Cleaning Validation
Documentation
Management
Iso Standards