| Distance: | Resume alert | Resumes 261 - 270 of 634 |
Student
Sterling, VA
... oFamiliarized with FDA and ISO standards for medical devices. 3-D Biomechanical Eye Modeling Using Patient-Specific MRI Images JAN 2019 – MAY 2020 ●Constructing 3D biomechanical eye models and using them to quantify specific morphological parameters ... - 2020 Aug 13
... oFamiliarized with FDA and ISO standards for medical devices. 3-D Biomechanical Eye Modeling Using Patient-Specific MRI Images JAN 2019 – MAY 2020 ●Constructing 3D biomechanical eye models and using them to quantify specific morphological parameters ... - 2020 Aug 13
Assistant Medical Device
College Park, MD
... ● Product development management, Double-barrel syringe study, FDA documentation, prepare and test samples of modified biopolymer, organize and perform animal studies, optimization of protocol and preclinical studies relating to antibacterial ... - 2020 Aug 07
... ● Product development management, Double-barrel syringe study, FDA documentation, prepare and test samples of modified biopolymer, organize and perform animal studies, optimization of protocol and preclinical studies relating to antibacterial ... - 2020 Aug 07
Lean Six Engineering
Hyattsville, MD
... Drafted the biocompatible shell to encapsulate the electronics, using MED610, adhering to the FDA regulations. Generated results by simulating the conical spring structure, for tissue attachment, in COMSOL. ADDITIONAL EXPERIENCE As a Special Events ... - 2020 Jul 25
... Drafted the biocompatible shell to encapsulate the electronics, using MED610, adhering to the FDA regulations. Generated results by simulating the conical spring structure, for tissue attachment, in COMSOL. ADDITIONAL EXPERIENCE As a Special Events ... - 2020 Jul 25
DATABASE ADMIN
Alexandria, VA
... • Involved in Validating FDA regulated systems • Involved in scripting, security, space management, jobs scheduling and maintenance, etc. • Created Work instructions document for SQL Server 2012,2008R2 server installation, upgrade and apply patches. ... - 2020 Jun 30
... • Involved in Validating FDA regulated systems • Involved in scripting, security, space management, jobs scheduling and maintenance, etc. • Created Work instructions document for SQL Server 2012,2008R2 server installation, upgrade and apply patches. ... - 2020 Jun 30
Office Assistant Engineering
Washington, DC
... (ADVAMED) Washington, DC Policy and Investment Analyst Intern, AdvaMed Accel June 2019 – December 2019 Developed a series of FDA Best Practices Guides to educate AdvaMed’s small company members on how to prepare for and manage premarket regulatory ... - 2020 Jun 23
... (ADVAMED) Washington, DC Policy and Investment Analyst Intern, AdvaMed Accel June 2019 – December 2019 Developed a series of FDA Best Practices Guides to educate AdvaMed’s small company members on how to prepare for and manage premarket regulatory ... - 2020 Jun 23
Medical Project Management, Senior Project Coordinator
Alexandria, VA
... Lundbeck Research USA, Paramus NJ September 2013 – November 2015 Research Assistant Supported the differentiation of novel antidepressant Trintellix (vortioxetine) - awarded FDA label claim for improving cognition in MDD patients in May 2018 ... - 2020 May 28
... Lundbeck Research USA, Paramus NJ September 2013 – November 2015 Research Assistant Supported the differentiation of novel antidepressant Trintellix (vortioxetine) - awarded FDA label claim for improving cognition in MDD patients in May 2018 ... - 2020 May 28
Oracle, AWS, SQL Server, Sybase, Unix, Scripting, OO Languages
Largo, MD, 20774
... Food and Drug Administration – development of a toxicology report approval system (10/1998 – 04/1999) Architected HTML with JavaScript pages to assist in drug approvals workflow processing for the Food and Drug Administration (FDA). US Department of ... - 2020 Apr 24
... Food and Drug Administration – development of a toxicology report approval system (10/1998 – 04/1999) Architected HTML with JavaScript pages to assist in drug approvals workflow processing for the Food and Drug Administration (FDA). US Department of ... - 2020 Apr 24
Medical Clinical Research
Rockville, MD
... Provide a medical opinion regarding medical based questions, legal and regulatory matters, based on the CMS regulations, FDA regulations, HIPAA compliance Provide a communication between clinicians, researchers and IT specialists involved in the ... - 2020 Apr 12
... Provide a medical opinion regarding medical based questions, legal and regulatory matters, based on the CMS regulations, FDA regulations, HIPAA compliance Provide a communication between clinicians, researchers and IT specialists involved in the ... - 2020 Apr 12
Project Manager
Vienna, VA
... Client: FDA Alfresco Customization/Development for FDA CSTAR(Center Submission Tracking and Reporting) Developing custom model in alfresco which includes customization of Aspects/Permissions/Behavior model of the system. Developing custom Datalists ... - 2020 Apr 10
... Client: FDA Alfresco Customization/Development for FDA CSTAR(Center Submission Tracking and Reporting) Developing custom model in alfresco which includes customization of Aspects/Permissions/Behavior model of the system. Developing custom Datalists ... - 2020 Apr 10
Manager Chemical Engineering
Washington, DC
... Prepared technology transfers documents, protocols and SOPs for regulatory submission to FDA-CBER. Developed a process to manage data reporting clinical records for Post- Marketing Surveillance Study. 1997-1997 GLAXOSMITHKLINE, Inc., Raleigh, NC, ... - 2020 Apr 05
... Prepared technology transfers documents, protocols and SOPs for regulatory submission to FDA-CBER. Developed a process to manage data reporting clinical records for Post- Marketing Surveillance Study. 1997-1997 GLAXOSMITHKLINE, Inc., Raleigh, NC, ... - 2020 Apr 05