| Distance: | Resume alert | Resumes 471 - 480 of 642 |
Oracle Data
Rockville, MD
... Weekly meetings with FDA key users. Overall system reduced drug approval time at the FDA from 3 years to 6 months. RS Information Systems Inc. . 03/25/1996 – 04/10/2000 Senior Systems Programmer Analyst Arlington, VA Develop the Integrated Naval ... - 2014 Feb 25
... Weekly meetings with FDA key users. Overall system reduced drug approval time at the FDA from 3 years to 6 months. RS Information Systems Inc. . 03/25/1996 – 04/10/2000 Senior Systems Programmer Analyst Arlington, VA Develop the Integrated Naval ... - 2014 Feb 25
Senior Oracle Programmer Analyst - Senior Oracle Developer
MD, 20746
... Worked as a Programmer Analyst on contract with the Food and Drug Administration (FDA), Public Health Service, U.S. Department of Health and Human Services. . Provided Oracle 4GL v 6.0, SQL*Forms 3.0, SQL*Plus, PL*SQL, and Oracle programming support ... - 2014 Feb 19
... Worked as a Programmer Analyst on contract with the Food and Drug Administration (FDA), Public Health Service, U.S. Department of Health and Human Services. . Provided Oracle 4GL v 6.0, SQL*Forms 3.0, SQL*Plus, PL*SQL, and Oracle programming support ... - 2014 Feb 19
Project Manager Quality Control
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
... • 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
Quality Assurance Management
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
... 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
Medical Safety
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
... 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
Management Manager
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
... 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
Customer Service Assistant
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
... 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
Oracle Engineer
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
... 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
Design Engineering
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
... 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
Engineer Project Manager
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
... 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