2001 -2008 Manager, Regulatory Affairs @ Care Products, Inc.
Paul Swift Education
The Johns Hopkins University
Master's Degree (Biotechnology)
Northwestern University - Kellogg School of Management
(RAPS Executive Development)
Loyola University Maryland
Bachelor's Degree (BS, Biology)
Paul Swift Skills
FDA
Regulatory Affairs
Medical Devices
Regulatory Submissions
Regulatory Requirements
Design Control
Medical Diagnostics
CE marking
CAPA
Validation
PMA
IVD
V&V
Medical Device Directive
ISO 14971
Infectious Diseases
21 CFR
Premarket Approval (PMA)
Biotechnology
ISO 13485
Clinical Trials
U.S. Food and Drug Administration (FDA)
Corrective and Preventive Action (CAPA)
Public Speaking
Sales
Strategy
Premarket Approval Pma
u.s. Food and Drug Administration Fda
Microsoft Word
Research
Pharmaceutical Industry
Crossfunctional Team Leadership
Corrective and Preventive Action Capa
Project Management
Customer Service
Change Management
Marketing
Management
Training
u.s. Food and Drug Administration
Premarket Approval
Corrective and Preventive Action
Paul Swift Summary
Paul Swift, based in Texas, United States, is currently a Head of Regulatory and Clinical Affairs, Americas at ZEISS Medical Technology. Paul Swift brings experience from previous roles at Alcon and BD. Paul Swift holds a Master's Degree in Biotechnology @ The Johns Hopkins University. With a robust skill set that includes FDA, Regulatory Affairs, Medical Devices, Regulatory Submissions, Regulatory Requirements and more. Paul Swift has 2 emails on RocketReach.
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