Chad Herrman

Manager @Unilever

Redding, CT, US
EMAILS
c••••••••@unilever.com
MOBILE NUMBERS
+18•••••••39

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WORK HISTORY

Dec 2021 — Present

Manager @Unilever

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Trumbull, CT, US

Team and technical lead Chromatography & Mass Spectrometry supporting primarily applied R&D. Provide additional technical support for early technology projects when needed. Responsibilities include but are not limited to chemical characterization, impurity profiling, identification of unknowns, method development and validation for targeted components, stability study director, SOP writing, report review, development of laboratory staff, build 3P platforms for advanced measurements, and expansion of lab capabilities.

EDUCATION

2002 — 2005

Illinois Institute of Technology

Masters, Analytical Chemistry

1995 — 1999

University of Illinois Urbana-Champaign

B.S., Chemistry

SKILLS

Electrospray IonizationElisaLc-Ms/MsAnalytical TechniquesValidationMass SpectrometryGmpElectrochemcialMulti-Dimensional ChromatographyContaminant AnalysisLaboratoryRp-HplcLiquid Chromatography-Mass Spectrometry (Lc-Ms)R&DMethod DevelopmentFluorescenceLc-MsTrace QuantitationChemical IonizationSpeTitrationChromatographyRaw Material CharacterizationUv/VisHilicCharacterizationSpectroscopyUplcHplcPhotoionizationElsdAnalytical Chemistry

ABOUT CHAD HERRMAN

Scientist, Chromatographer, Mass Spectrometrist, and Innovator-I am an experienced Analytical Chemist with experience across the pharmaceutical, cosmetics/personal care, and environmental industries. I lead by example and build networks across internal teams and external partners to solve problems and push innovations through the pipeline. Specialties: Analytical Chemist with extensive experience in separation sciences including: LC/MS,LC/MS/MS, and HPLC. Experience with triple quadrupole, ion trap, and Q-TOF MS systems from various vendors. Other analytical skills include: multi-dimensional chromatography, ELISA analysis, AA, flame photometry, UV/VIS, SPE, FIA/continuous flow analysis. Strong background in method development and validation of LC/MS, LC/MS/MS, and HPLC. Extensive experience with small molecules from multiple classes, as well peptides/proteins, and naturally derived raw materials. Familiar with ICH, GMP, and GLP guidelines. Experience with statistical software programs for chemoinformatics and modeling.

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