2009 -2012 Sr. Associate Process Development Engineer II @ Grifols Therapeutics Inc.
2007 -2009 Validation Specialist II @ Talecris Biotherapeutics
now Process and Validation Engineer @
now Process and Validation Engineering Technician II @
Christopher Goodwin Education
North Carolina State University
Master (Statistics)
2021-2025
North Carolina State University
B.S.ChE (Chemical Engineering)
1996-2001
Christopher Goodwin Skills
Project Management
Validation
GMP
Filtration
Aseptic Processing
Cleaning Validation
FDA
Biotechnology
Process Simulation
Biopharmaceuticals
Pharmaceutical Industry
CAPA
Change Control
Chemical Engineering
GxP
Equipment/Process Startup and Shakedown
Equipment Commissioning and Qualification
Writing SOPs and Batch Records
Sterilization
Lyophilization
V&V
Aseptic Technique
Cross-functional Team Leadership
FDA GMP
Lifesciences
Manufacturing
Quality Auditing
Quality System
R
Sop
Technical Writing
Vaccines
Trackwise
Technology Transfer
Software Documentation
Purification
Protein Chemistry
Medical Devices
Life Sciences
LIMS
HPLC
GLP
GAMP
Fermentation
Design of Experiments
Computer System Validation
21 CFR Part 11
Communication
Public Speaking
Christopher Goodwin Summary
Christopher Goodwin, based in Knightdale, NC, US, is currently a Sr. Principal Associate - QA Compliance at Eli Lilly and Company. Christopher Goodwin brings experience from previous roles at SpringWorks Therapeutics, Catalent Pharma Solutions, Robling Medical, Inc. and Novo Nordisk. Christopher Goodwin holds a 2021 - 2025 Master in Statistics @ North Carolina State University. With a robust skill set that includes Project Management, Validation, GMP, Filtration, Aseptic Processing and more. Christopher Goodwin has 2 emails and 1 mobile phone numbers on RocketReach.
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