Director QA Analytical and Stability @ (June 2019 - June 2022)
Manager, Stability and Statistics @ (January 2012 - January 2015)
Associate Director Quality, Stability and Statistics @ (January 2015 - June 2022)
Manager, Stability and Statistics @ (January 2012 - January 2015)
Quality Control Scientist II @ (September 2010 - January 2012)
Sr QA Compliance Specialist @ (January 2006 - January 2010)
Director Of Quality Assurance and Manager @ Avatar Pharmaceutical Services (May 2003 - December 2006)
Consultant @ (September 2002 - February 2003)
Director Biomedical Operations and Program Director and Clinical Studies Coordinator @ (January 1998 - January 2001)
Manager of Contract Research @ PerSeptive Biosystems, Inc. (January 1998 - January 2001)
Manager of In Vitro Diagnostics Development and Senior Scientist @ (January 1987 - January 1993)
Scientist @ (January 1987 - January 1987)
Scientist and Technician @ Baxter Travenol (Clinical Assays) (January 1984 - January 1986)
Technician and Intern @ Reagents Applications (January 1983 - January 1983)
Lorraine Murphy Education
UC San Diego
Bachelor of Science (BS) (Chemistry and Political Science)
Lorraine Murphy Skills
GLP
FDA
GMP
Validation
Biotechnology
Cleaning Validation
Lifesciences
Quality Assurance
Document Management
CAPA
Sop
Technology Transfer
Auditing
ISO
V&V
Quality System
Chromatography
HPLC
Pharmaceutical Industry
Clinical Development
Lorraine Murphy Summary
Lorraine Murphy, based in Chelmsford, MA, US, is currently a Director, CMC Quality Assurance at Enanta Pharmaceuticals. Lorraine Murphy brings experience from previous roles at Akebia Therapeutics, Sanofi and Genzyme. Lorraine Murphy holds a Bachelor of Science (BS) in Chemistry and Political Science @ UC San Diego. With a robust skill set that includes GLP, FDA, GMP, Validation, Biotechnology and more. Lorraine Murphy has 1 emails and 1 mobile phone numbers on RocketReach.
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