| Resume alert | Resumes 41 - 50 of 163 |
Executive Office Administration / Data Entry / Client Relations
Mukilteo, WA
... FDA contact for Serial Number tracking. Planner / Buyer 08/2004 to 02/2005 Fluke - Kelly Services – Everett, Washington Order and expedite component parts from outside vendors and internal suppliers to support manufacturing operations. Troubleshoot ... - 2018 Aug 20
... FDA contact for Serial Number tracking. Planner / Buyer 08/2004 to 02/2005 Fluke - Kelly Services – Everett, Washington Order and expedite component parts from outside vendors and internal suppliers to support manufacturing operations. Troubleshoot ... - 2018 Aug 20
Medical Assistant Coding
Federal Way, WA
... Collecting all the medical data for oncology physician for presenting the patient in the tumor board Assisting physician with medical records to get approved from FDA drugs for cancer patient. Extensive research work on cancer patients documents ... - 2018 Aug 03
... Collecting all the medical data for oncology physician for presenting the patient in the tumor board Assisting physician with medical records to get approved from FDA drugs for cancer patient. Extensive research work on cancer patients documents ... - 2018 Aug 03
Test Cases Engineer
Redmond, WA
... Strong familiarity with FDA regulations including Part 11 and PDMA FDA regulations(pharma) and FDA 21 CFR Part 820 regulated medical device manufacturing environments for the devices, Process Validation including IQ, OQ and PQ, under the Quality ... - 2018 Jun 18
... Strong familiarity with FDA regulations including Part 11 and PDMA FDA regulations(pharma) and FDA 21 CFR Part 820 regulated medical device manufacturing environments for the devices, Process Validation including IQ, OQ and PQ, under the Quality ... - 2018 Jun 18
Chemical Engineering Medical
Kenmore, WA
... DEC 07 – JUN 09 Prepare regulatory documentation for Institutional Review Board (IRB) approval, IDE and the clinical trial sites in compliance with FDA regulations (medical device). Create and maintain SOPs and cGMP for the project with feedback ... - 2018 Jun 02
... DEC 07 – JUN 09 Prepare regulatory documentation for Institutional Review Board (IRB) approval, IDE and the clinical trial sites in compliance with FDA regulations (medical device). Create and maintain SOPs and cGMP for the project with feedback ... - 2018 Jun 02
Analyst, microsoft Office, type 70wpm, documentation, gathering requi
Federal Way, WA, 98023
... June-Oct 2012 Worked on the development of the business and functional requirements and specifications for a new paperless platform to process medical clinic trials for the independent review board and FDA approval process in an Agile environment. ... - 2018 May 01
... June-Oct 2012 Worked on the development of the business and functional requirements and specifications for a new paperless platform to process medical clinic trials for the independent review board and FDA approval process in an Agile environment. ... - 2018 May 01
SAS programmer
Kenmore, WA
... Mapped locations of cigarette sales to minors during FDA retail-outlet inspections using ArcGIS. Created 2015 Pennsylvania Department of Health Regional Primary Contractor Youth Tobacco Survey (YTS) Report. Drafted a preliminary factsheet using SAS ... - 2018 Apr 08
... Mapped locations of cigarette sales to minors during FDA retail-outlet inspections using ArcGIS. Created 2015 Pennsylvania Department of Health Regional Primary Contractor Youth Tobacco Survey (YTS) Report. Drafted a preliminary factsheet using SAS ... - 2018 Apr 08
Manager Microsoft Office
Bothell, WA
... Managing accountable materials in accordance with FDA and ISO standards and analyzing floor production demand. Generated continual product stream support through continual advancements in production line support improvements and streamlining ... - 2017 Dec 15
... Managing accountable materials in accordance with FDA and ISO standards and analyzing floor production demand. Generated continual product stream support through continual advancements in production line support improvements and streamlining ... - 2017 Dec 15
Manager Development
Seattle, WA
... Broad regulatory writing experience that includes: authoring influential white papers submitted to the EMA, GLP toxicology study reports and program summaries, Investigator Brochures, INDs, and questions to be submitted to the FDA. Capable of ... - 2017 Oct 04
... Broad regulatory writing experience that includes: authoring influential white papers submitted to the EMA, GLP toxicology study reports and program summaries, Investigator Brochures, INDs, and questions to be submitted to the FDA. Capable of ... - 2017 Oct 04
Professional Experience Engineering
Kirkland, WA, 98034
... Skills: Proficient with MATLAB, C,C++, JAVA, LabVIEW, Visual Studio 2012, and CAD software, Filemaker Pro, Computer Aided Transcription System (CATS), NEURON In-depth knowledge of FDA (21 CFR part 820), ISO 13785, 15189, IEC 60601, IEC/TR 80002 and ... - 2017 Sep 12
... Skills: Proficient with MATLAB, C,C++, JAVA, LabVIEW, Visual Studio 2012, and CAD software, Filemaker Pro, Computer Aided Transcription System (CATS), NEURON In-depth knowledge of FDA (21 CFR part 820), ISO 13785, 15189, IEC 60601, IEC/TR 80002 and ... - 2017 Sep 12
Quality Customer Service
Bothell, WA
... ●Inspected and tested telemetry controls and measured small parts using MicroView equipment in the production of implantable defibrillators under FDA requirements. ●Maintained the monitoring and recording processes for the environmental chamber ... - 2017 Sep 11
... ●Inspected and tested telemetry controls and measured small parts using MicroView equipment in the production of implantable defibrillators under FDA requirements. ●Maintained the monitoring and recording processes for the environmental chamber ... - 2017 Sep 11