Senior Principal @ (November 2024 - December 2025)
Principal @ (September 2022 - November 2024)
CMC Writer @ (September 2019 - September 2022)
R and D Manager @ (February 2018 - September 2019)
Senior Project Manager @ (September 2013 - February 2018)
Manager, Pharmaceutical Sciences @ (May 2012 - April 2013)
Scientist II @ (January 2011 - May 2012)
Scientist I @ Wolfe Laboratories, Inc. (August 2007 - December 2010)
Senior Manager, Pharmaceutical Sciences @ (May 2013 - August 2013)
Scott Michaels Education
University of Kansas
MSc with Honors (Pharmaceutical Chemistry)
2010-2013
McGill University
Bachelor of Science (B.Sc.) (Chemistry, Pharmacology)
2002-2007
Scott Michaels Skills
Drug Development
HPLC
LC/MS/MS
Formulation Development
ADME
GMP
GLP
Drug Metabolism
Pharmacokinetics
Solid State Characterization
Analytical Chemistry
Project Management
Pharmaceutical Sciences
Drug Discovery
Chemistry
Protein Chemistry
Formulation
LC-MS
UV/Vis
Biotechnology
SOP
Pharmaceutical Industry
Peptides
Chromatography
Drug Delivery
Technology Transfer
U.S. Food and Drug Administration (FDA)
Validation
Life Sciences
Research and Development (R&D)
Standard Operating Procedure (SOP)
Research and Development R&d
Lc Ms
Program Management
Standard Operating Procedure Sop
Solid State
u.s. Food and Drug Administration Fda
Product Launch
Sales
Research
u.s. Food and Drug Administration
Standard Operating Procedure
Research and Development
Scott Michaels Summary
Scott Michaels, based in Cody, WY, US, is currently a Director, Biopharma Regulatory Affairs at Global Regulatory Writing & Consulting (GLOBAL). Scott Michaels brings experience from previous roles at Global Regulatory Writing & Consulting (GLOBAL) and Cody Laboratories, Inc.. Scott Michaels holds a 2010 - 2013 MSc with Honors in Pharmaceutical Chemistry @ University of Kansas. With a robust skill set that includes Drug Development, HPLC, LC/MS/MS, Formulation Development, ADME and more. Scott Michaels has 1 emails and 2 mobile phone numbers on RocketReach.
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