| Distance: | Resume alert | Resumes 441 - 450 of 645 |
Human Resources Management
Arlington, VA
... Primary sectors are Healthcare IT (HHS, CMS, CDC, MHS, DHHQ, NIH, FDA), Financial (IRS, SEC) and Federal Civilian (DOC, NOAA, FAA, DOS, Dept. of ED, DHS). 2020 Company, LLC (Acquired by Acentia) Falls Church, Virginia January 2007 to April 2012 ... - 2015 Jul 01
... Primary sectors are Healthcare IT (HHS, CMS, CDC, MHS, DHHQ, NIH, FDA), Financial (IRS, SEC) and Federal Civilian (DOC, NOAA, FAA, DOS, Dept. of ED, DHS). 2020 Company, LLC (Acquired by Acentia) Falls Church, Virginia January 2007 to April 2012 ... - 2015 Jul 01
Customer Service Sales
Arlington, VA
... May 2012 – September 2013 Machine Operator § Thorough understanding of capsule production process Complete FDA batch records accurately for running products Set up for production Adequate knowledge of basic tool use Disassembling for cleaning Work ... - 2015 May 29
... May 2012 – September 2013 Machine Operator § Thorough understanding of capsule production process Complete FDA batch records accurately for running products Set up for production Adequate knowledge of basic tool use Disassembling for cleaning Work ... - 2015 May 29
Manager Medical
Herndon, VA
... MHRA or FDA GLP regulations) Published various types of submissions for drugs and devices, including INDs, NDAs, 510(k)s (in CTD/eCTD format) - original submissions and lifecycle support (including Annual Reports, Amendments, and Supplements) ... - 2015 May 04
... MHRA or FDA GLP regulations) Published various types of submissions for drugs and devices, including INDs, NDAs, 510(k)s (in CTD/eCTD format) - original submissions and lifecycle support (including Annual Reports, Amendments, and Supplements) ... - 2015 May 04
Regulatory Affairs
Washington, DC
... • Thorough understanding of FDA regulations/ICH guidelines, budget terms and concepts, and scientific terminology and testing procedure requirements. - 2015 May 03
... • Thorough understanding of FDA regulations/ICH guidelines, budget terms and concepts, and scientific terminology and testing procedure requirements. - 2015 May 03
Development Product
Washington, DC
... ● Participated in regulatory meetings and activities including dossier development, drug submissions, and FDA correspondence. ● Reviewed and verified production Records including protocols, reports, processes and data. ● Performed inspections and ... - 2015 Mar 30
... ● Participated in regulatory meetings and activities including dossier development, drug submissions, and FDA correspondence. ● Reviewed and verified production Records including protocols, reports, processes and data. ● Performed inspections and ... - 2015 Mar 30
Manager Training
Virginia
... Kept records for all federally regulated safety and sanitation programs as the Safety director, ensuring compliance to programs such as OSHA, FDA, and DEA . Launched innovative solutions for reducing costs, decreasing waste, enhancing inventory ... - 2015 Mar 25
... Kept records for all federally regulated safety and sanitation programs as the Safety director, ensuring compliance to programs such as OSHA, FDA, and DEA . Launched innovative solutions for reducing costs, decreasing waste, enhancing inventory ... - 2015 Mar 25
Software Engineer Test
Alexandria, VA
... Boston Scientific Contractor 2011-2012 Test Automation Lead Member of the Integration and Test team writing C# tests for FDA validation of Windows based deep brain stimulation application. Contractor for Neuromodulation Group of Boston Scientific. C ... - 2015 Mar 11
... Boston Scientific Contractor 2011-2012 Test Automation Lead Member of the Integration and Test team writing C# tests for FDA validation of Windows based deep brain stimulation application. Contractor for Neuromodulation Group of Boston Scientific. C ... - 2015 Mar 11
Medical Data
Virginia
... to FDA requests), and ICH integrated clinical reports for client organizations Oversaw research (e.g., literature searches, FDA and ICH regulations and guidelines) related to scientific, medical and regulatory documents/filings/submissions. ... - 2015 Feb 18
... to FDA requests), and ICH integrated clinical reports for client organizations Oversaw research (e.g., literature searches, FDA and ICH regulations and guidelines) related to scientific, medical and regulatory documents/filings/submissions. ... - 2015 Feb 18
Management Project
Virginia
... proficient in FDA, Good Clinical Practice (GCP), Good Laboratory Practice (GLP), and Good Manufacturing Practice (GMP) requirements. Research & Projects: Demonstrated success investigating novel biotechnology / drug candidates. Adept at designing ... - 2015 Feb 14
... proficient in FDA, Good Clinical Practice (GCP), Good Laboratory Practice (GLP), and Good Manufacturing Practice (GMP) requirements. Research & Projects: Demonstrated success investigating novel biotechnology / drug candidates. Adept at designing ... - 2015 Feb 14
Quality Engineer Engineering
Dunn Loring, VA
... Experience in pharmaceutical industry with solid knowledge on FDA 21 CFR Part 11: Electronic records and Electronic signatures, 21 CFR Part 50, **, **, ***, ***, 312, 314, 820 . Quality Engineer experience in analysis of corrective action, process ... - 2015 Feb 04
... Experience in pharmaceutical industry with solid knowledge on FDA 21 CFR Part 11: Electronic records and Electronic signatures, 21 CFR Part 50, **, **, ***, ***, 312, 314, 820 . Quality Engineer experience in analysis of corrective action, process ... - 2015 Feb 04