Armen Shamirian

Associate Director of Analytical Development and Qc @Nurix Therapeutics

San Francisco, CA, US
EMAILS
a••••••••@nurixtx.com
MOBILE NUMBERS
+18•••••••75

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WORK HISTORY

May 2025 — Present

Associate Director of Analytical Development and Qc @Nurix Therapeutics

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San Francisco, CA, US

EDUCATION

N/A

University of Guilan

Bachelor of Science - BS, Chemistry

2008 — 2010

Amirkabir University of Technology - Tehran Polytechnic

M.Sc., Analytical Chemistry

N/A

University of Wisconsin-Madison

Drug Product Development Certificate Program, Pharmaceutical Sciences

2012 — 2016

University of Illinois Chicago

Doctor of Philosophy (Ph.D.), Analytical Chemistry and Nanotechnology

SKILLS

High-Performance Liquid Chromatography (Hplc)GmpPowder X-Ray DiffractionLiquid Chromatography-Mass Spectrometry (Lc-Ms)DlsAnalytical Method ValidationLaboratoryGas ChromatographyChemistrySpectroscopyPersonal CareFormulationUv/Vis SpectroscopyIrAnalytical Methods DevelopmentAnalytical ChemistryCosmeticsMaterialsNmrNuclear Magnetic Resonance (Nmr)SurfactantsFluorescence SpectroscopyR&DMethod DevelopmentUv-VisUv/VisGc-MsResearch and Development (R&D)Raw MaterialsGood Laboratory Practice (Glp)ChromatographyChemical EngineeringChemicalsResearchHplcTga

ABOUT ARMEN SHAMIRIAN

SummaryAn accomplished and motivated Analytical scientist and lead with over 12 years of industrial experience. Knowledgeable in CMC development and a subject matter expert in a variety of analytical and material characterization techniques. An Accountable leader who can instill his team loyalty and commitment by mentoring and modeling through actions. Creates a positive work environment by creating a vision and providing strong support for growth.Expertise• Advanced understanding of pharmaceutical material science and its impact on drug product performance and manufacturing• Group leader, including management and professional development responsibilities for direct reports• Knowledgeable in CMC development across all phases of drug development from initial regulatory filings through registration, validation, and launch• Strong knowledge in Analytical characterization and control for solid oral drug products• Direct experience with analytical method development, validation, transfer, and stability evaluations• Extensive knowledge and significant hands-on experience with analytical techniques including UPLC, GC, MS spectrometry, KF, UV-Vis, FT-IR, Fluorescence Spectroscopy, AAS, TGA/DSC, PSA, SEM-EDS, and TEM• Demonstrates potential for technical proficiency, creativity, collaboration with others, and independent thought• Excellent written and verbal communication skills and organizational skills as well as the ability to prioritize and manage multiple tasks under tight timelines• Knowledgeable in Quality by Design (QbD) and Process Analytical Technology (PAT) principles • Experienced working with controlled substances under DEA regulations

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