2008 -2013 Principal Associate Regulatory Affairs @
2006 -2007 Regulatory Operations Coordinator @
2004 -2006 Regulatory Affairs Specialist @
2002 -2004 Regulatory Affairs Associate @
1999 -2002 Chemistry Research Associate @
Bem Atsma Education
Worcester Polytechnic Institute
Master’s Degree (Bioscience Administration)
2014-2017
UC San Diego 2013-2013
University of the Fraser Valley
(Statistics)
2009-2010
University of Victoria
BSc (Chemistry)
1993-1999
Bem Atsma Skills
Chemistry
Regulatory Affairs
eCTD
Regulatory Submissions
FDA
IND
GMP
Sop
Biotechnology
Pharmaceutical Industry
CMC
CAPA
Clinical Development
Clinical Trials
Drug Development
GCP
Lifesciences
NDA
Oncology
Regulatory Requirements
Validation
Quality System
Global Application Support
Stability
Technology Transfer
GLP
GxP
Regulatory Documentation
CMC Regulatory Affairs
CRO
Life Sciences
Good Clinical Practice (GCP)
U.S. Food and Drug Administration (FDA)
Corrective and Preventive Action (CAPA)
Electronic Common Technical Document (eCTD)
Technology
Regulatory
Good Clinical Practice Gcp
Corrective And Preventive Action Capa
Human Rights
Pmda
U.S. Food And Drug Administration Fda
Leading Meetings
Electronic Common Technical Document Ectd
Science
Animal Welfare
u.s. Food and Drug Administration
Good Clinical Practice
Electronic Common Technical Document
Corrective and Preventive Action
Bem Atsma Summary
Bem Atsma, based in Boston, MA, US, is currently a Director, Regulatory Affairs CMC at bluebird bio. Bem Atsma brings experience from previous roles at Biogen, Genzyme and AnorMED Corp.. Bem Atsma holds a 2014 - 2017 Master’s Degree in Bioscience Administration @ Worcester Polytechnic Institute. With a robust skill set that includes Chemistry, Regulatory Affairs, eCTD, Regulatory Submissions, FDA and more. Bem Atsma has 2 emails and 4 mobile phone numbers on RocketReach.
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