Staci L. Anderson

R&D Documentation and Quality Specialist | Pharmaceuticals, Dietary Supplements | Technical writing, data analysis and review, cGMP quality compliance, CMC regulatory documentation

Role
R & d Quality Associate at Reckitt
Location
Salt Lake City, UT, US
LinkedIn followers
500 followers
Manufacturing & ProductionView LinkedIn profile

About Staci L. Anderson

Skilled in current Good Manufacturing Practices (cGMP), technical writing, change…

Experience

  1. R & d Quality Associate

    Reckitt

    Mar 2025 — Present · Salt Lake City, UT, US

Education

  • Utah State University

    Bachelor of Science degree

Skills

  • Training
  • Ftir
  • Gas Chromatography
  • Cleaning Validation
  • Gxp
  • Waters Empower Analytical Software
  • High-Performance Liquid Chromatography (Hplc)
  • Quality Control
  • Gmp
  • Test Methodologies
  • Standard Operating Procedure (Sop)
  • 21 Cfr Part 11
  • Validation
  • Cgmp Practices
  • Dissolution
  • Mentoring
  • Laboratory Information Management System (Lims)
  • Pharmaceutical Manufacturing
  • Gc
  • Pharmaceutical Industry
  • Sop
  • Fda
  • Regulatory Affairs
  • Glp
  • Usp
  • Trackwise
  • Change Control
  • U.s. Food and Drug Administration (Fda)
  • Lims
  • Analytical Chemistry
  • U.s. Title 21 Cfr Part 11 Regulation
  • Medical Devices
  • Capa
  • Technical Writing
  • Hplc
  • Good Laboratory Practice (Glp)
  • Team Leadership
  • Laboratory
  • Dissolution Testing
  • Chromatography

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