2018 -2022 Director, Global Regulatory Affairs – CMC Biologics @
2016 -2018 Senior Principal Scientist, Drug Product Manufacturing Science and Technology @
2015 -2016 Quality Assessment Lead @
2014 -2015 Acting Team Leader @
2013 -2014 Senior CMC Reviewer and QbD Liaison @
2010 -2013 CMC Reviewer @
2006 -2010 Senior Formulation Scientist @
2002 -2006 Instructor @
1998 -2000 Assistant Professor @ China State Institute of Pharmaceutical Industry (CSIPI)
Daniel Peng Education
UTHSC College of Pharmacy
Postdoctoral Fellow (Industrial Pharmacy)
2000-2002
West China University of Medical Sciences
Doctor of Philosophy (Ph.D.) (Pharmaceutics)
1993-1998
Xi'an Medical University
B.S. (Pharmacy)
1989-1993
Daniel Peng Skills
Quality by Design
Pharmaceutical Industry
FDA
Question based Review (QbR)
Design of Experiments
Artificial Neural Networks
Multivariate Analysis
CMC Regulatory Affairs
Formulation Development
Pharmaceutcial Process Development
Biodegradable polymeric delivery system
Nanoparticles
Compression and compaction
HPLC
Formulation
Pharmaceutics
Chemistry
Validation
Sop
Technology Transfer
Drug Delivery
Analytical Chemistry
GMP
Regulatory Affairs
Biotechnology
Regulatory Submissions
Leadership
Question Based Review Qbr
Process Improvement
Strategic Planning
Program Management
U.S. Food And Drug Administration Fda
Management
Question Based Review
Artificial Neural
Compression
Liaison
CMC
Pharmaceutcial Process
Biodegradable Polymeric
u.s. Food and Drug Administration
Daniel Peng Summary
Daniel Peng, based in Philadelphia, PA, US, is currently a Executive Director, Regulatory Affairs CMC at Insmed Incorporated. Daniel Peng brings experience from previous roles at Checkpoint Therapeutics Inc, Merck and Shire. Daniel Peng holds a 2000 - 2002 Postdoctoral Fellow in Industrial Pharmacy @ UTHSC College of Pharmacy. With a robust skill set that includes Quality by Design, Pharmaceutical Industry, FDA, Question based Review (QbR), Design of Experiments and more. Daniel Peng has 2 emails on RocketReach.
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