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Washington, DC
... 1 • Conduct aggregated safety analyses of phase 1, 2 and 3 clinical trials and draft response to ad hoc queries from FDA, EMEA and other global regulatory agencies and medical communications. • Perform aggregate safety analysis of adverse event (AEs ...
- 2014 Feb 05
Waldorf, MD
... Employment History: Deloitte & Touche April 2013 - Present Fixed Asset Consultant Rosslyn, VA • Oversaw the Food and Drug Administration (FDA) Office of Information Management (OIM) ITAM task order project deliverable to generate a requirements ...
- 2014 Jan 18
Fairfax, VA
... Food and Drug Administration (FDA) protocol; executed O157 and non- O157 E. coli strains which produce toxin; used precise mechanisms for detection of toxin by using Shiga Toxin Quik Chek testing techniques and O157 Quik Chek testing techniques. ...
- 2014 Jan 16
District Heights, MD
... Experience consulting/contracting with clients from both private and public sectors: Quest Diagnostics Inc, US Food and Drug Administration (FDA), Verizon Wireless, Naval Sea Systems command (NAVSEA), Military Traffic Management Command (MTMC), ...
- 2013 Dec 11
Greenbelt, MD
... staining, Western blotting, DSC, Instron mechanical testing Relevant Coursework “QSR Compliance Basics: Complying with the FDA's Medical Device 21 CFR 820 Quality System Regulation” EduQuest, Frederick, MD April 30-May 1, 2013 Introduction to cGMP ...
- 2013 Dec 09
Arlington, VA
... Test Engineer Booz Allen Hamilton (FDA) Date– July 2012 - October 2012 • Piloted hands-on customer training of modernized document management system 1 • Devised Requirements Traceability Matrix, Master Test Plan, and Test Specifications • Directed ...
- 2013 Dec 04
Hyattsville, MD
... of Health and Human Services - Federal and Drug Administration (FDA) Help Desk Support Analyst Provided a full range of Tier-1 service desk support to the generic drug facilities and sites required to abide by new regulations as established by the ...
- 2013 Nov 26
Arlington, VA
... Streamlining of preclinical drug design Designed and performed a study of lung cancer producing a computational method assessing a potential of a gene to express a successful anti-cancer drug target, resulting in 6-fold enrichment in FDA-approved ...
- 2013 Nov 23
Centreville, VA
... also to be used as a model for capacity studies in all areas going forward Selected to lead a lab-wide effort to reduce dependence on Research Use Only reagents, whose elimination by the FDA would severely impact patient care Selected by the ...
- 2013 Oct 31
Woodbridge, VA
... Lab operations, under FDA / c HACCP and FSIS (Pathogen Reduction). Evaluation of plant process based on GMP (Good Manufacture Practices) and HACCP reg. Experienced working in environmental chemistry physical-chemical and microbiological analysis of ...
- 2013 Oct 07