If you need more lookups,
subscriptions start at $34 USD/month.
Deb Rasmussen Location
Raritan, NJ, US
Deb Rasmussen Work
Regulatory Affairs Senior Director @ (January 2003 - Present)
Executive Director Regulatory Affairs @ Ortho Clinical Diagnostics (November 2009 - September 2010)
WW Executive Director Regulatory Affairs @ Johnson & Johnson (Ortho-Clinical Diagnostics) (January 2008 - January 2010)
World wide Executive Director Regulatory Affairs @ Veridex (March 2003 - November 2009)
VP Regulatory and Quality Affairs @ Visible Genetics (January 2000 - January 2003)
Director Quality Assurance @ Chiron Diagnostics (January 1995 - January 1998)
Director Quality @ (January 1991 - January 1995)
QC manager @ (January 1986 - January 1989)
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 5 emails and 2 mobile phone numbers on RocketReach.
Looking for a different Deb Rasmussen?
Find contact details for 700 million professionals.