Adria Tyndall

Director, Regulatory CMC at Novartis

Role
Director, Regulatory Affairs Cmc at Novartis
Location
Chicago, IL, US
LinkedIn followers
500 followers

About Adria Tyndall

Regulatory Scientist experienced in pharmaceutical regulatory strategy, intelligence and…

Experience

  1. Director, Regulatory Affairs Cmc

    Novartis

    Jun 2019 — Present

    Regulatory CMC lead for Commercial Gene Therapy (Zolgensma) at Novartis Gene Therapies (formerly AveXis). Within Novartis, supported additional Cell and Gene therapy programs through contract manufacturing initiatives and network transformations.

Education

  • The Johns Hopkins University

    Master of Science - MS, Regulatory Science

    2013 — 2017

  • University of Minnesota

    Bachelor of Science (B.S.), Chemistry

    1998 — 2003

Skills

  • Hplc
  • Validation
  • Gas Chromatography
  • Uv/Vis
  • Ftir
  • Dissolution
  • Sop
  • Fda
  • Titration
  • Lifesciences
  • Karl Fischer
  • Ion Chromatography
  • Empower
  • Analytical Method Validation
  • Technical Writing
  • Method Transfer
  • Data Review
  • Change Control
  • Capa
  • Gmp
  • Instrumentation
  • Pharmaceutical Industry
  • Regulatory Affairs
  • Uv
  • Analytical Chemistry
  • Dionex
  • Assay Development
  • Laboratory
  • Quality Control
  • R&D
  • Raw Materials
  • Chromatography
  • Quality Auditing
  • Pharmaceutics
  • 21 Cfr Part 11
  • Chromeleon
  • Instrument Troubleshooting
  • Cmc Regulatory Affairs
  • Licensing
  • Fda Gmp

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Adria Tyndall — Director, Regulatory Affairs Cmc at Novartis in Chicago, IL, US | Unifers