ANGELIQUE FIONA DUPONT

**** ****** ****** ? Wheat Ridge, CO ? 80033

Cell: 512-***-**** ? acp1nk@r.postjobfree.com

Qualifications

? Five years in a GMP and GLP laboratory as a quality control chemist

? Experience with array of analytical instruments and software platforms including HPLC, HPLC-Mass Spectrometer, GC, Flame AA, Ion Chromatograph, UV-VIS Spectrometer, Karl Fischer Titrators and their platforms

? Troubleshooting and maintenance of HPLCs

? Work in a high-paced API pharmaceutical manufacturing environment

Education

University of Texas- Austin, TX

Bachelor of Science: Chemistry (2006- 2010)

Professional Experience

Agilent Technologies- Contract laboratory for custom oligonucleotide synthesis. Manufacturer of GMP and non-GMP material for pre-clinical and clinical applications, Boulder, CO;

Quality Control Analyst- Entry; July 2010 ? December 2013

Quality Control Analyst- Intermediate; December 2013- present

? Perform analytical testing for the process, release, and stability of APIs

? Skillful with Agilent 1100/1200/1260 Series HPLC, Agilent 1290 UHPLC, Waters Alliance HPLC platforms, including operation, troubleshooting, and repair

? Proficient with Agilent OpenLab and ChemStation software, and Waters Empower Chromatographic Data Systems, including custom report building

? Experience with HPLC Mass Spectrometry, utilizing Agilent single quadrupole, and Agilent Flame AA and software

? Knowledge of Bruker NMR operation, used for small molecule analysis such as raw materials purity testing

? Proficient with UV-Vis Spectrometry, Metrohm and Mettler Toledo Karl Fischer titration, pH, and IR analysis

? Serve as subject matter expert for the Dionex/Thermo Ion Chromatograph, utilizing Chromeleon software

? Performed microbiology testing of cleaning validation samples for endotoxin and bioburden

? Help train new employees and colleagues with analytical instruments and company processes

? Lead analyst for manufacturing campaigns and quality control representation for the coordination of projects with supervisors, project managers, and the client

? Review and update standard operating procedures, protocols, reports, and analytical methods

? Use of deviations, change controls, investigations, CAPAs, and inquiries systems

? Work in a GMP and GLP environment

? Daily use of Microsoft Office: Word, Excel, Access, and Powerpoint as well as Regulatory Asset Manager software

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