Armen Shamirian
Associate Director of Analytical Development and Qc @Nurix Therapeutics
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WORK HISTORY
Associate Director of Analytical Development and Qc @Nurix Therapeutics
San Francisco, CA, US
EDUCATION
University of Guilan
Bachelor of Science - BS, Chemistry
Amirkabir University of Technology - Tehran Polytechnic
M.Sc., Analytical Chemistry
University of Wisconsin-Madison
Drug Product Development Certificate Program, Pharmaceutical Sciences
University of Illinois Chicago
Doctor of Philosophy (Ph.D.), Analytical Chemistry and Nanotechnology
SKILLS
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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