Daniel Peng Location

Philadelphia, PA, US

Daniel Peng Work

  • 2018 - 2022 Director, Global Regulatory Affairs – CMC Biologics @ Merck
  • 2016 - 2018 Senior Principal Scientist, Drug Product Manufacturing Science and Technology @ Shire
  • 2015 - 2016 Quality Assessment Lead @ FDA
  • 2014 - 2015 Acting Team Leader @ FDA
  • 2013 - 2014 Senior CMC Reviewer and QbD Liaison @ FDA
  • 2010 - 2013 CMC Reviewer @ FDA
  • 2006 - 2010 Senior Formulation Scientist @ AstraZeneca

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

Daniel Peng Summary

Daniel Peng, based in Philadelphia, PA, US, is currently a VP, Regulatory Affairs CMC at Checkpoint Therapeutics Inc. Daniel Peng brings experience from previous roles at Insmed Incorporated, 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 3 emails and 2 mobile phone numbers on RocketReach.

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