| Distance: | Resume alert | Resumes 311 - 320 of 634 |
Manager Operations
Springfield, VA
... Manage, support, record and edit WebEx and Adobe web conferences that may include over 1000 participants Webcast meetings for FDA through adobe and WebEx Scorpion DJ & Catering January 2006 - June 2013 Dj Equipment set up Projector Installation and ... - 2018 Oct 10
... Manage, support, record and edit WebEx and Adobe web conferences that may include over 1000 participants Webcast meetings for FDA through adobe and WebEx Scorpion DJ & Catering January 2006 - June 2013 Dj Equipment set up Projector Installation and ... - 2018 Oct 10
Clinical Research Manager
Washington, DC
... Food and Drug Administration (FDA) regulations, Good Clinical Practices (GCP) and International Conference on Harmonization (ICH) guidelines and Company related Standard Operation Procedures (SOPs) EDUCATION SHAW UNIVERSITY, RALEIGH, NC Bachelor of ... - 2018 Sep 26
... Food and Drug Administration (FDA) regulations, Good Clinical Practices (GCP) and International Conference on Harmonization (ICH) guidelines and Company related Standard Operation Procedures (SOPs) EDUCATION SHAW UNIVERSITY, RALEIGH, NC Bachelor of ... - 2018 Sep 26
Manager Management
Rockville, MD
... Spearhead the multiple Prime awards at FDA, HUD, and DC Govt. Responsible for the company’s day-to-day operating activities, including revenue and sales growth; expense, cost and margin control; and monthly, quarterly and annual financial goal ... - 2018 Sep 17
... Spearhead the multiple Prime awards at FDA, HUD, and DC Govt. Responsible for the company’s day-to-day operating activities, including revenue and sales growth; expense, cost and margin control; and monthly, quarterly and annual financial goal ... - 2018 Sep 17
Quality Training
Silver Spring, MD
... Perform audits of clinical sites, vendors against GCP/cGMP standards, FDA requirements and other regulatory standards and ensure resolution of any identified issues. Perform external audits of suppliers/vendors Review complaints and quality event ... - 2018 Sep 14
... Perform audits of clinical sites, vendors against GCP/cGMP standards, FDA requirements and other regulatory standards and ensure resolution of any identified issues. Perform external audits of suppliers/vendors Review complaints and quality event ... - 2018 Sep 14
Manager Project
Centreville, VA
... design, development, integration, testing, and deployment for the State of Texas including 27 state agencies and two large data centers under Health Insurance Portability and Accountability Act (HIPAA) and Federal Drug Administration (FDA) mandates. ... - 2018 Sep 11
... design, development, integration, testing, and deployment for the State of Texas including 27 state agencies and two large data centers under Health Insurance Portability and Accountability Act (HIPAA) and Federal Drug Administration (FDA) mandates. ... - 2018 Sep 11
Management Manager
Rockville, MD
... Contract management experience with Federal agencies such as DOD, DOA, DOJ, DOE, USAID, VA, FDA, USDA, NARA, NOAA, FBI, DHS, NCI, as well as HHS and its lower tier branches such as NIH, DMID, NHLBI, NCI, NCCAM, NEI, NIAID, NICHD, NIDCR, NIMH, NINDS, ... - 2018 Sep 11
... Contract management experience with Federal agencies such as DOD, DOA, DOJ, DOE, USAID, VA, FDA, USDA, NARA, NOAA, FBI, DHS, NCI, as well as HHS and its lower tier branches such as NIH, DMID, NHLBI, NCI, NCCAM, NEI, NIAID, NICHD, NIDCR, NIMH, NINDS, ... - 2018 Sep 11
Test Cases Project
Silver Spring, MD
... Permanent Resident Work Experience: Sapient Govt services Sr Automation Tester/ Lead July 2017- Till date Client: FDA Projects: VIA - Inspection Application and TIMS- Inspection Application The objective of this project is regulated by FDA ... - 2018 Sep 10
... Permanent Resident Work Experience: Sapient Govt services Sr Automation Tester/ Lead July 2017- Till date Client: FDA Projects: VIA - Inspection Application and TIMS- Inspection Application The objective of this project is regulated by FDA ... - 2018 Sep 10
Design Engineer Engineering
McLean, VA
... •Thorough knowledge of ASME Y14.5 principles and Design Controls, FDA’s QSR and ISO regulations and GLP guidelines specially 21 CFR 820, ISO 13485, ISO 11608, IEC 60601 and 510(k) requirements and review process. Proven track record of consistently ... - 2018 Sep 05
... •Thorough knowledge of ASME Y14.5 principles and Design Controls, FDA’s QSR and ISO regulations and GLP guidelines specially 21 CFR 820, ISO 13485, ISO 11608, IEC 60601 and 510(k) requirements and review process. Proven track record of consistently ... - 2018 Sep 05
Assistant Manager
Silver Spring, MD
... (Forestville, MD) ● Ensure operation of donor center is compliant with company SOPs, State and Federal (FDA) regulations, OSHA, CLIA ● Maintain up to date training records ● Hire, train, and coordinate onboarding process for new employees ● ... - 2018 Aug 17
... (Forestville, MD) ● Ensure operation of donor center is compliant with company SOPs, State and Federal (FDA) regulations, OSHA, CLIA ● Maintain up to date training records ● Hire, train, and coordinate onboarding process for new employees ● ... - 2018 Aug 17
Sales Management
Great Falls, VA
... (Currently Aethlon Medical, NASDAQ: AEMD) San Diego, California Built company from a research idea into an operating company and guided it through the first FDA clinical trials. Raised $3.5 million of capital. Assembled a distinguished board of ... - 2018 Aug 13
... (Currently Aethlon Medical, NASDAQ: AEMD) San Diego, California Built company from a research idea into an operating company and guided it through the first FDA clinical trials. Raised $3.5 million of capital. Assembled a distinguished board of ... - 2018 Aug 13