Global Regulatory Team Lead @ (November 2019 - November 2022)
Regulatory Lead @ Bioverativ, a Sanofi company (August 2018 - January 2020)
Senior Manager, Regulatory Affairs @ (January 2016 - August 2018)
CMC Regulatory Submissions Manager @ (July 2015 - December 2015)
Senior Regulatory Associate, Global Clinical Trials @ Cubist Pharmaceuticals (October 2014 - June 2015)
Senior Associate I, Regulatory Operations @ Cubist Pharmaceuticals (June 2012 - October 2014)
Senior Associate I, Regulatory Operations @ (February 2008 - June 2012)
Associate II, Regulatory Operations @ (January 2006 - February 2008)
Senior Assistant II @ (March 2001 - January 2006)
Matt Millstein Education
Clark University
Bachelor Of Arts (Communications)
1996-2000
Matt Millstein Skills
Strategic Planning
Social Media
Biotechnology
Regulatory Affairs
Regulatory Submissions
Manufacturing
Training
Chemistry
Marketing
Pharmaceutical Industry
Leadership
Clinical Trials
Regulatory Operations
eCTD
Life Sciences
NDA
Drug Development
Document Management
Clinical Development
U.S. Food And Drug Administration Fda
Electronic Common Technical Document Ectd
Standard Operating Procedure Sop
FDA
Sop
IND
Biopharmaceuticals
New Drug Application Nda
Electronic Submissions
Standard Operating Procedure
u.s. Food and Drug Administration
New Drug Application
Electronic Common Technical Document
Matt Millstein Summary
Matt Millstein, based in Boston, MA, US, is currently a Director, Regulatory Affairs at Morphic Therapeutic. Matt Millstein brings experience from previous roles at Sanofi Genzyme, Bioverativ, a Sanofi company, Stealth BioTherapeutics and Shire. Matt Millstein holds a 1996 - 2000 Bachelor Of Arts in Communications @ Clark University. With a robust skill set that includes Strategic Planning, Social Media, Biotechnology, Regulatory Affairs, Regulatory Submissions and more. Matt Millstein has 2 emails and 1 mobile phone numbers on RocketReach.
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