Chris Brisco

Project Lead The Way at Texarkana Arkansas Schools
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Contact Information
us****@****om
(386) 825-5501
Location
Texarkana, Texas, United States, US
Skills

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5.0

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Letitia Mozeke

Chris has a vast knowledge of the manufacturing and production industry along with extensive knowledge of regulatory policies and procedures. Working with him I have found him to be both professional and credible. He has been tremdously helpful and a pleasure to work with. I would highly recommend him because he goes above and beyond the realm of his job to assist when needed.

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Experience

  • Texarkana Arkansas Schools
    • United States
    • Education Administration Programs
    • 1 - 100 Employee
    • Project Lead The Way
      • Jul 2020 - Present

      IDE, POE, CEA, Robotics

    • Robotics/ Business/ CTC
      • Aug 2018 - Jul 2020

    • Facilitator
      • Aug 2017 - Aug 2018

      EAST Lab Facilitator

  • cGMP / 503B Consultant
    • Regulatory Consultant
      • Jul 2013 - Jul 2020

      21 CFR 210/211, GMP, USP 795/797, Microbiology, Purified Water/ Water Treatment, ISO Classified Clean Room, IQ/OQ/PQ, Cleaning Validation, Analytical Method Development/Validation, Quality Systems, FDA Audit Preparation, Process Design, EPA, TCEQ, Site Remediation 21 CFR 210/211, GMP, USP 795/797, Microbiology, Purified Water/ Water Treatment, ISO Classified Clean Room, IQ/OQ/PQ, Cleaning Validation, Analytical Method Development/Validation, Quality Systems, FDA Audit Preparation, Process Design, EPA, TCEQ, Site Remediation

  • Vogue International a Johnson & Johnson Company
    • United States
    • Personal Care Product Manufacturing
    • 1 - 100 Employee
    • Regulatory Affairs Consultant
      • Oct 2016 - Apr 2017

      cGMP SME, alignment with global supply network. Export testing, DOT materials classification, microbiology SME. cGMP SME, alignment with global supply network. Export testing, DOT materials classification, microbiology SME.

  • Pharma Nobis
    • United States
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Director of Technical and Regulatory Affairs
      • Aug 2008 - Sep 2012

      Maintain cGMP, EPA, and FDA compliance for facility. Including label copy information and claims, new product acceptability, hazardous waste disposition, special projects. Maintain cGMP, EPA, and FDA compliance for facility. Including label copy information and claims, new product acceptability, hazardous waste disposition, special projects.

  • Humco Holding Group
    • Manager Pharmaceutical Manufacturing
      • Sep 2007 - Aug 2008

  • Pharma Nobis
    • United States
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Product Development
      • Jan 2005 - Aug 2007

      Product development, OTC Pharma and H&H product development from concept to bench to scale up and into full production. Method development for API's.

    • Chemist
      • Aug 1998 - Jan 2005

      Chemist testing USP products and raw materials. Testing USP products using GC, HPLC, Uv, FTIR, and standard methods of analysis.

  • Rineco
    • Chemist
      • Jan 1997 - Aug 1997

      Trace Metals, TCLP, Cold Mercury Analysis, HPLC, GC, FIMS, ICP, AA. Trace Metals, TCLP, Cold Mercury Analysis, HPLC, GC, FIMS, ICP, AA.

Education

  • Texas A&M University-Texarkana
    MSBA, Business
    2003 - 2005
  • Henderson State University
    BS, Chemistry
    1991 - 1997

Community

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