| Distance: | Resume alert | Resumes 371 - 380 of 638 |
Project Management Sales
Sterling, VA
... Our business relationships included: IRS, FDA, Networking groups in community, Dept. of Labor, Service SOR, Capital Visitors Center, Ft. Belvoir, City of Alexandria, Fairfax County Government, GoodWill, Salvation Army and many others. Successful at ... - 2017 Jul 11
... Our business relationships included: IRS, FDA, Networking groups in community, Dept. of Labor, Service SOR, Capital Visitors Center, Ft. Belvoir, City of Alexandria, Fairfax County Government, GoodWill, Salvation Army and many others. Successful at ... - 2017 Jul 11
Manager Management
Rockville, MD
... Responsible for updating American Medical Association drug database on FDA new drug approvals. oSr. Programmer Analyst, Ciber Inc., McLean, V - (02/1999 – 08/2001) – Multiple client engagements. oSr. Programmer Analyst EMC/Millennia III, Connecticut ... - 2017 Jul 07
... Responsible for updating American Medical Association drug database on FDA new drug approvals. oSr. Programmer Analyst, Ciber Inc., McLean, V - (02/1999 – 08/2001) – Multiple client engagements. oSr. Programmer Analyst EMC/Millennia III, Connecticut ... - 2017 Jul 07
Manager Test Cases
Washington, DC
... ● Tested application with FDA regulations for software validation, 21 CFR Part 11, and G(X) P. ● Updated and maintained Software Compliance SOP’s. ● Conducted Facility inspections and Method audits according to schedule ● Managed defects with QC ● ... - 2017 Jul 05
... ● Tested application with FDA regulations for software validation, 21 CFR Part 11, and G(X) P. ● Updated and maintained Software Compliance SOP’s. ● Conducted Facility inspections and Method audits according to schedule ● Managed defects with QC ● ... - 2017 Jul 05
Test Cases
Reston, VA
... Developed and tested FDA compliance requirements pertaining to CFR 21 part 11 with regards to electronics signature. Maintained Requirement Traceability Matrices to measure the testing progress Interfaced with developers in resolving the defects ... - 2017 Jun 27
... Developed and tested FDA compliance requirements pertaining to CFR 21 part 11 with regards to electronics signature. Maintained Requirement Traceability Matrices to measure the testing progress Interfaced with developers in resolving the defects ... - 2017 Jun 27
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