| Distance: | Resume alert | Resumes 431 - 440 of 641 |
Data Manager
Falls Church, VA
... Standardized the pharmaceutical files from the third party (DEA, FDA, and State) and SAP database systems using the rule set in Standardize stage (Quality Stage). Data Profiling and cleansing the controlled substance files from the State, DEA and ... - 2015 Sep 24
... Standardized the pharmaceutical files from the third party (DEA, FDA, and State) and SAP database systems using the rule set in Standardize stage (Quality Stage). Data Profiling and cleansing the controlled substance files from the State, DEA and ... - 2015 Sep 24
Technician Management
Silver Spring, MD
Henry Joseph Consultant - FDA Silver Spring, MD *************@*****.*** - 301-***-**** Brings a positive attitude to the table with the ability to multitask and prioritize responsibilities while keeping a professional manner. Willing to relocate: ... - 2015 Sep 21
Henry Joseph Consultant - FDA Silver Spring, MD *************@*****.*** - 301-***-**** Brings a positive attitude to the table with the ability to multitask and prioritize responsibilities while keeping a professional manner. Willing to relocate: ... - 2015 Sep 21
Microsoft Office Medical
Garrett Park, MD
... Cytometer, Western Blot, PCR, and many other analytes Thorough understanding of Good Clinical Laboratory Practice (GCLP), FDA, & GLP Able to work independently and as a cooperative team member Constantly seeking new skills to optimize set career ... - 2015 Aug 24
... Cytometer, Western Blot, PCR, and many other analytes Thorough understanding of Good Clinical Laboratory Practice (GCLP), FDA, & GLP Able to work independently and as a cooperative team member Constantly seeking new skills to optimize set career ... - 2015 Aug 24
Technical Writer
Arlington, VA
... Critical Environment documentation at the Bristol-Myers Squibb LSCC facility Played an integral part in BMS passing their FDA pre-inspection with zero deficiencies Technical Writer – Contract 06/2011 to 10/2011 DRS ICAS, LLC Merrimack, NH Created ... - 2015 Aug 18
... Critical Environment documentation at the Bristol-Myers Squibb LSCC facility Played an integral part in BMS passing their FDA pre-inspection with zero deficiencies Technical Writer – Contract 06/2011 to 10/2011 DRS ICAS, LLC Merrimack, NH Created ... - 2015 Aug 18
Executive Assistant
Washington, DC
... – July 2014 Regulatory/Quality Ops/Contracts Specialist In this position I was responsible for the review and editing of all internal and external documents of acceptable quality required for submissions to the FDA in paper and electronic format. ... - 2015 Aug 13
... – July 2014 Regulatory/Quality Ops/Contracts Specialist In this position I was responsible for the review and editing of all internal and external documents of acceptable quality required for submissions to the FDA in paper and electronic format. ... - 2015 Aug 13
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 Manager
Ashburn, VA
... Built a strong relations with vendors to improve operation cost for goods and services Defined and implemented FDA-compliant food safety program and trained food handlers to maintain high standards of cleanliness, safety, and quality. Developed ... - 2015 Jun 11
... Built a strong relations with vendors to improve operation cost for goods and services Defined and implemented FDA-compliant food safety program and trained food handlers to maintain high standards of cleanliness, safety, and quality. Developed ... - 2015 Jun 11
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