| Distance: | Resume alert | Resumes 371 - 380 of 634 |
Medical Technical Support
Falls Church, VA
... PLM knowledge, multi task handling ability with the knowledge of EU Medical Device Regulations in compliance with relevant standards like: ISO13485, 93/42/EEC Life Sciences: US FDA regulations 21 CFR Part 11 (210/211, 150, 56, 58, 311, 314, 820), ... - 2017 Jun 27
... PLM knowledge, multi task handling ability with the knowledge of EU Medical Device Regulations in compliance with relevant standards like: ISO13485, 93/42/EEC Life Sciences: US FDA regulations 21 CFR Part 11 (210/211, 150, 56, 58, 311, 314, 820), ... - 2017 Jun 27
Customer Service Manager
Washington, DC
... Green Leadership Scholarship, 2013, 2015 College of Undergraduate Studies, Featured Author, October 2014 College of Undergraduate Studies, Public Service, Published, March 2015 MedStar Certified, FDA Research Coordinator, 2013 MedStar Centricity EMR ... - 2017 Jun 26
... Green Leadership Scholarship, 2013, 2015 College of Undergraduate Studies, Featured Author, October 2014 College of Undergraduate Studies, Public Service, Published, March 2015 MedStar Certified, FDA Research Coordinator, 2013 MedStar Centricity EMR ... - 2017 Jun 26
Engineer Computer Science
Reston, VA
... Analyze FDA data center migration proposal and requirements. Design, Review and Validating new data center software architecture. Research new technology compatibilities. Working with development team to migrate, configure and debugging legacy ... - 2017 Jun 21
... Analyze FDA data center migration proposal and requirements. Design, Review and Validating new data center software architecture. Research new technology compatibilities. Working with development team to migrate, configure and debugging legacy ... - 2017 Jun 21
Professional Experience Medical
Derwood, MD, 20855
... preparation Medical Information Collaboration with Marketing Initiatives CMC documents including stability reports and assay validation Authored FDA briefing documents for meetings PROFESSIONAL EXPERIENCE Consultant/Contractor BioPharm Global, Inc. ... - 2017 May 31
... preparation Medical Information Collaboration with Marketing Initiatives CMC documents including stability reports and assay validation Authored FDA briefing documents for meetings PROFESSIONAL EXPERIENCE Consultant/Contractor BioPharm Global, Inc. ... - 2017 May 31
Interpreter Training
Fairfax, VA, 22030
... Assistance Committee projects, US Congress 2007, 2008, 2009, 2010, 2012 Interpreter for Food and Drug Administration (FDA) inspection in Indonesia, August 2009 Simultaneous interpreter for Rule of Law program for Indonesian law enforcement ... - 2017 May 24
... Assistance Committee projects, US Congress 2007, 2008, 2009, 2010, 2012 Interpreter for Food and Drug Administration (FDA) inspection in Indonesia, August 2009 Simultaneous interpreter for Rule of Law program for Indonesian law enforcement ... - 2017 May 24
Integration solution architect
Reston, VA
... It involves integration with Salesforce, 3rd party legacy systems, SAP, FDA, master data hubs etc. Integrating systems Salesforce, Lionbridge (Language Translation), FDA Electronic Submission gateway, SAP, Product and Customer data hubs Solution ... - 2017 May 17
... It involves integration with Salesforce, 3rd party legacy systems, SAP, FDA, master data hubs etc. Integrating systems Salesforce, Lionbridge (Language Translation), FDA Electronic Submission gateway, SAP, Product and Customer data hubs Solution ... - 2017 May 17
Project Management Quality Assurance
Fairfax, VA
... 2003 Food and Drug Administration (FDA) ● Subject Matter Expert for analysis of software systems development process at an Agency level. ● Designed agency-wide System Development Life-Cycle (SDLC) compliant with OMB 300 requirements and in ... - 2017 May 15
... 2003 Food and Drug Administration (FDA) ● Subject Matter Expert for analysis of software systems development process at an Agency level. ● Designed agency-wide System Development Life-Cycle (SDLC) compliant with OMB 300 requirements and in ... - 2017 May 15
Management Manager
Washington, DC
... Food & Drug Administration White Oak, MD Records Management Subject Matter Expert Supported the development and establishment of a clear and unified direction for FDA Records Management Program• Address targeted needs for electronically stored ... - 2017 May 04
... Food & Drug Administration White Oak, MD Records Management Subject Matter Expert Supported the development and establishment of a clear and unified direction for FDA Records Management Program• Address targeted needs for electronically stored ... - 2017 May 04
Enterprise Architecture, Data Architecture, Data Warehousing, Data Man
Potomac, MD
... OTHER POSITIONS HELD at SRA Lead Enterprise Architect / Technical Lead for NIH May 2004 – Oct 2005 Senior NIH Requirement Analyst Jan 2004 –May 2004 SRA FDA Data Warehouse Architect Sept 2002 – Dec 2004 SRA CDC Project/Test Engineer Jan 2000 – Aug ... - 2017 May 01
... OTHER POSITIONS HELD at SRA Lead Enterprise Architect / Technical Lead for NIH May 2004 – Oct 2005 Senior NIH Requirement Analyst Jan 2004 –May 2004 SRA FDA Data Warehouse Architect Sept 2002 – Dec 2004 SRA CDC Project/Test Engineer Jan 2000 – Aug ... - 2017 May 01
Project Test Cases
Herndon, VA, 20170
... Environment: Windows XP/Windows 2003, UNIX,ALM, Oracle, Quality Center, J2EE, XML, Web Services, JavaScript, HTML, XML, PVCS, Oracle, MS Project and MS Office FDA, Rockville, MD Jan’06 - Sep’07 Role: QA Analyst Project: Devices Registration and ... - 2017 Apr 27
... Environment: Windows XP/Windows 2003, UNIX,ALM, Oracle, Quality Center, J2EE, XML, Web Services, JavaScript, HTML, XML, PVCS, Oracle, MS Project and MS Office FDA, Rockville, MD Jan’06 - Sep’07 Role: QA Analyst Project: Devices Registration and ... - 2017 Apr 27