Huston Howell

Huston Howell

Associate Director and Head of Quality Assurance at Leadiant Biosciences, Inc.

Role
Associate Director and Head of Quality Assurance at Leadiant Biosciences, Inc
Location
Washington, DC, US
LinkedIn followers
500 followers

About Huston Howell

More than 20 years of cumulative regulatory affairs and manufacturing quality experience in the U. S. pharmaceutical industry, working with commercial companies and as a consultant.

Experience

  1. Associate Director and Head of Quality Assurance

    Leadiant Biosciences, Inc

    Jul 2020 — Present · Gaithersburg, MD, US

Education

  • University of Tennessee, Knoxville

    Ph.D., Analytical Chemistry

    1979 — 1983

Skills

  • Analytical Chemistry
  • Regulatory Requirements
  • Regulatory Affairs
  • Ind
  • Pharmaceutics
  • Chromatography
  • 21 Cfr Part 11
  • Standard Operating Procedure (Sop)
  • Quality System
  • V&V
  • Cleaning Validation
  • U.s. Food and Drug Administration (Fda)
  • Biopharmaceuticals
  • Technology Transfer
  • Glp
  • Validation
  • Gxp
  • Lims
  • Quality Auditing
  • Chemistry
  • Pharmacovigilance
  • Gmp
  • Capa
  • Vaccines
  • Hplc
  • Regulatory Submissions
  • Biotechnology
  • Pharmaceutical Industry
  • Sop
  • Fda
  • Change Control

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