2009 -2010 Executive Director Regulatory Affairs @ Ortho Clinical Diagnostics
2008 -2010 WW Executive Director Regulatory Affairs @ Johnson & Johnson (Ortho-Clinical Diagnostics)
2003 -2009 World wide Executive Director Regulatory Affairs @ Veridex
2000 -2003 VP Regulatory and Quality Affairs @ Visible Genetics
1995 -1998 Director Quality Assurance @ Chiron Diagnostics
1991 -1995 Director Quality @
1986 -1989 QC manager @
Deb Rasmussen Education
University of California, Berkeley
Deb Rasmussen Skills
Regulatory Submissions
FDA
Medical Devices
Pharmaceutical Industry
Regulatory Affairs
ISO 13485
Biotechnology
Clinical Development
Hardware Diagnostics
GMP
GCP
Healthcare
Cross-functional Team Leadership
Quality System
PMA
Quality Assurance
Quality Auditing
Quality Control
V&V
Regulatory Requirements
Technology Transfer
U.S. Food and Drug Administration (FDA)
Sales
Regulatory
Cross Functional Team Leadership
U.S. Food And Drug Administration Fda
Research
Inspection
Leadership
u.s. Food and Drug Administration
Deb Rasmussen Summary
Deb Rasmussen, based in Raritan, NJ, US, is currently a Regulatory Affairs Senior Director at Johnson & Johnson Company. Deb Rasmussen brings experience from previous roles at Ortho Clinical Diagnostics, Johnson & Johnson (Ortho-Clinical Diagnostics), Veridex and Visible Genetics. Deb Rasmussen holds a University of California, Berkeley. With a robust skill set that includes Regulatory Submissions, FDA, Medical Devices, Pharmaceutical Industry, Regulatory Affairs and more. Deb Rasmussen has 4 emails and 2 mobile phone numbers on RocketReach.
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