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Pam Riggio Location
Lake Forest, IL, US
Pam Riggio Work
Director Regulatory Affairs @ (December 2020 - Present)
Director of Regulatory Affairs @ (June 2015 - July 2020)
Regulatory Affairs Manager @ (January 2012 - June 2015)
Regulatory Affairs Manager @ First Priority, Inc. (January 2011 - January 2012)
Regulatory Product Manager @ (April 2006 - October 2010)
Global Project Manager @ Baxter Healthcare Corporation (January 2005 - January 2006)
Regulatory Affairs Associate @ Takeda Global Research and Development (January 1999 - January 2005)
Regulatory Affairs Associate @ (January 1993 - January 1999)
Pam Riggio Education
Drexel University College of Medicine
MS (Clinical Research Organization and Management)
2007-2009
DePaul University
BA
2003-2005
Pam Riggio Skills
Developing Regulatory Strategy
Regulatory Product Development
Regulatory Operations
Regulatory Strategy
Product Development
FDA
Pharmaceuticals
GMP
Regulatory Affairs
Clinical Development
Regulatory Requirements
ICH-GCP
Sop
Regulatory Submissions
Software Documentation
CAPA
21 CFR Part 11
Change Control
Biotechnology
GCP
Drug Development
Computer System Validation
Clinical Trials
Quality Assurance
eCTD
Biopharmaceuticals
Aseptic Processing
Regulations
Medical Writing
CRO
Medical Devices
Pharmaceutical Industry
Pharmacovigilance
R&D
Strategy
Therapeutic Areas
Validation
Pharmaceutics
U.S. Food and Drug Administration (FDA)
Pam Riggio Summary
Pam Riggio, based in Lake Forest, IL, US, is currently a Director Regulatory Affairs at Ora, Inc.. Pam Riggio brings experience from previous roles at PharMEDium Services, LLC, First Priority, Inc. and Hospira, Inc.. Pam Riggio holds a 2007 - 2009 MS in Clinical Research Organization and Management @ Drexel University College of Medicine. With a robust skill set that includes Developing Regulatory Strategy, Regulatory Product Development, Regulatory Operations, Regulatory Strategy, Product Development and more. Pam Riggio has 3 emails and 3 mobile phone numbers on RocketReach.
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