| | | 20,000+ Fresh Resumes Monthly | |
|
|
| |
Click here or scroll down to respond to this candidateCandidate's Name
Street Address
Cell: PHONE NUMBER AVAILABLE EMAIL AVAILABLE
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 PHONE NUMBER AVAILABLE 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
|
