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Resumes 481 - 490 of 649 |
Potomac, MD
... • Transferred technology from R&D to the Manufacturing Department on the Hepatitis B Virus HCII • projects as the result the FDA HPV approval in 1999. Improved product quality control by revising various Standard Operating Procedures for product ...
- 2014 Feb 17
Rockville, MD
... Effective lead of a team performing purification for phase I, II, III and clinical trial vaccines in a GMP/FDA regulated lab, finishing projects on time and within budget. Coordinated timelines and scheduling of projects as well as cost for ...
- 2014 Feb 06
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