Joan Beck

Role
Director, Regulatory Affairs at Phlow
Location
Greensboro, NC, US
LinkedIn followers
500 followers

About Joan Beck

25+ years of pharmaceutical experience in regulatory affairs and quality assurance;…

Experience

  1. Director, Regulatory Affairs

    Phlow

    Jan 2022 — Present

Skills

  • Sop
  • Pharmaceutics
  • Validation
  • Corrective and Preventive Action (Capa)
  • Sop Development
  • Quality Systems
  • Chemistry
  • Regulatory Submissions
  • Gxp
  • U.s. Food and Drug Administration (Fda)
  • Hplc
  • Compliance
  • Quality Auditing
  • Capa
  • Analytical Chemistry
  • Technology Transfer
  • Fda
  • Pharmaceutical Industry
  • Regulatory Requirements
  • Technical Writing
  • Lims
  • Quality System
  • Trackwise
  • Pharmaceuticals
  • Change Control
  • Standard Operating Procedure (Sop)
  • Quality Assurance
  • Quality Management
  • Ind
  • Cgmp
  • Drug Development
  • Fda Gmp
  • Regulatory Affairs
  • Auditing
  • Quality Control
  • Strategy
  • Manufacturing
  • Gmp
  • Nda

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Joan Beck — Director, Regulatory Affairs at Phlow in Greensboro, NC, US | Unifers