Paul Long

Paul Long has over 20 years of work experience in the pharmaceutical industry. Paul is currently working as the Director of Regulatory Affairs at SIGA Technologies, where they have been since 2015. Prior to this, they held positions at Actavis Laboratories UT, Inc., Watson Laboratories, Inc., Re, and Schwarz Pharma Manufacturing, Inc. At Actavis Laboratories UT, Inc., Paul served as the Director of Regulatory Affairs, overseeing the development of regulatory filing strategies and obtaining regulatory approval for product candidates. Paul also held the role of Associate Director, Regulatory Affairs at the same company, where they represented Regulatory Affairs on project teams and acted as the primary contact with regulatory agencies. At Watson Laboratories, Inc., Paul worked as a Manager of Regulatory Affairs, where they maintained regulatory filings and ensured compliance with regulatory requirements. Paul also served as a Regulatory Affairs Associate III at the same company, coordinating activities for regulatory filings and researching filing requirements. In their early career, Paul worked at Re as a Regulatory Affairs Associate II, where they coordinated activities for regulatory filings and maintained compliance with regulatory requirements. Prior to that, they worked as a Pharmaceutical Product Manager at Schwarz Pharma Manufacturing, Inc.

Paul Long has a Master of Business Administration (MBA) degree from the University of Utah, which they obtained from 2002 to 2004. Prior to that, they completed their Bachelor of Pharmacy (B.Pharm.) degree at Purdue University from 1993 to 1998. In addition, they hold a certification as "RAC certified," although further details regarding the institution and the year of obtaining the certification are not available.