Director, Regulatory, Quality, and Clinical Affairs @ Christie Medical Holdings, Inc. (August 2010 - January 2014)
Director, Clinical and Regulatory Affairs @ NovaLign Orthopaedics, Inc. (September 2008 - August 2010)
Sr. Manager, Clinical Affairs @ (March 2006 - September 2008)
Manager, Clinical Affairs @ ProRhythm, Inc. (January 2004 - February 2006)
Manager, Clinical Affairs @ (February 1999 - February 2004)
Eye and Tissue Bank Specialist @ (January 1993 - January 2003)
Dawn Norman Education
Southern Illinois University Edwardsville
MS (Biomedical Sciences and Chemistry)
1992-1995
Dawn Norman Skills
Regulatory Affairs
Clinical Trials
Clinical Research
Protocol
Biologics
FDA
Medical Devices
Regulatory Submissions
Lifesciences
Quality System
Design Control
ISO 13485
PMA
510k
Class I
Class II
Class III
CAPA
Compliance
IND
Biomedical Engineering
ISO 14971
Quality Assurance
Validation
CE marking
Change Control
21 CFR Part 11
Clinical Development
SOP
GMP
Life Sciences
U.S. Food and Drug Administration (FDA)
Corrective and Preventive Action (CAPA)
u.s. Food and Drug Administration Fda
Strategy
Regulatory
Consulting
Banking
u.s. Food and Drug Administration
Corrective and Preventive Action
Dawn Norman Summary
Dawn Norman, based in Memphis, TN, US, is currently a Partner at MRC Global. Dawn Norman brings experience from previous roles at MRC/X, LLC, Memphis Regulatory Consulting, LLC, Christie Medical Holdings, Inc. and NovaLign Orthopaedics, Inc.. Dawn Norman holds a 1992 - 1995 MS in Biomedical Sciences and Chemistry @ Southern Illinois University Edwardsville. With a robust skill set that includes Regulatory Affairs, Clinical Trials, Clinical Research, Protocol, Biologics and more. Dawn Norman has 2 emails and 2 mobile phone numbers on RocketReach.
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