Thomas Willi

Senior Analyst I at Raybow PharmaScience
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Contact Information
us****@****om
(386) 825-5501
Location
US
Languages
  • English -

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Experience

    • China
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Senior Analyst I
      • Sep 2021 - Present

      -Return to the bench for a more technical role

    • Interim Analytical Manager
      • Aug 2020 - Sep 2021

      - Responsible for training new chemists in cGMP methods and instrumentation- Responsible for directing work flow and ensuring projects stay on time

    • Analytical Chemist
      • Nov 2019 - Aug 2020

      -Responsible for method development/validation and release testing of Active Pharmaceutical Ingredients (APIs)-Provide analytical support for synthetic organic chemists including HPLC-MS and GC-MS

    • United States
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Research Associate, QC
      • Feb 2017 - Nov 2019

      -Responsible for release testing for Active Pharmaceutical Ingredients (APIs) (HPLC, GC, NMR, FTIR, DSC, and cKF) -Conduct testing for and implement new reference standards used in the QC laboratory Initiate and perform review of standard operating procedures (SOPs) -Coordinate testing with outside labs and oversee shipment of samples -Honored as a subject matter expert in DSC and TGA techniques -Responsible for release testing for Active Pharmaceutical Ingredients (APIs) (HPLC, GC, NMR, FTIR, DSC, and cKF) -Conduct testing for and implement new reference standards used in the QC laboratory Initiate and perform review of standard operating procedures (SOPs) -Coordinate testing with outside labs and oversee shipment of samples -Honored as a subject matter expert in DSC and TGA techniques

    • Formulation Scientist II
      • Jul 2015 - Feb 2017

      -Method Development -Manufacturing Process Development -Deformulation of Name Brand Pharmaceuticals -Analytical testing of R&D and Finished Product Samples -Method Development -Manufacturing Process Development -Deformulation of Name Brand Pharmaceuticals -Analytical testing of R&D and Finished Product Samples

    • United States
    • Pharmaceutical Manufacturing
    • 100 - 200 Employee
    • Associate Scientist
      • Mar 2015 - Jul 2015

      • Perform analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. • Perform analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing.

    • United States
    • Pharmaceutical Manufacturing
    • 100 - 200 Employee
    • Chemist I
      • Feb 2013 - Feb 2015

      • Test incoming raw materials (controlled and non-controlled substances) using specific chemical and physical tests including: Particle Size, Loss on Drying, Karl Fischer, Assays and Impurities (HPLC, UV, GC, and titrations), FTIR, Heavy Metals, Melting Point, Bulk and Tapped Density, Residue on Ignition, Conductivity and TLC • Cross-trained in Finished Product analytical techniques (Content Uniformity, Dissolution, etc.) • Trained in the used of Empower and LIMS software • Test incoming raw materials (controlled and non-controlled substances) using specific chemical and physical tests including: Particle Size, Loss on Drying, Karl Fischer, Assays and Impurities (HPLC, UV, GC, and titrations), FTIR, Heavy Metals, Melting Point, Bulk and Tapped Density, Residue on Ignition, Conductivity and TLC • Cross-trained in Finished Product analytical techniques (Content Uniformity, Dissolution, etc.) • Trained in the used of Empower and LIMS software

    • United States
    • Textile Manufacturing
    • 700 & Above Employee
    • Co-op
      • Jan 2009 - Dec 2009

      • Improved the carpet recycling process by writing SOPs and running tests for new machinery that improved output approximately 300% • Established more relevant specifications and tests for raw materials used in extrusion that are still being used. • Compiled data and performed statistical analysis of material properties in Microsoft Excel to ensure quality and prevent costly claims • Improved the carpet recycling process by writing SOPs and running tests for new machinery that improved output approximately 300% • Established more relevant specifications and tests for raw materials used in extrusion that are still being used. • Compiled data and performed statistical analysis of material properties in Microsoft Excel to ensure quality and prevent costly claims

    • Supplemental Instruction Leader
      • Aug 2006 - Dec 2008

      • Enjoyed tutoring students in entry level Chemistry and Physics • Responsible for making session plans and practice exams • Enjoyed tutoring students in entry level Chemistry and Physics • Responsible for making session plans and practice exams

Education

  • Clemson University
    MS, Bioengineering
    2010 - 2012
  • Clemson University
    BS, Polymer and Fiber Chemistry
    2005 - 2010

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