| Distance: | Resume alert | Resumes 301 - 310 of 641 |
Various - Program Management, VP Ops, Systems Engineer, CQO
Arlington, VA
... and maintained certifications for ISO 9001 and 13485, Health Canada Class II, and CE Mark (EU) and prepared for/initiated FDA approval, DoD Information Assurance Ann Unitas, PMP 703-***-**** ***.******@*****.*** Certification and Accreditation ... - 2019 Jun 10
... and maintained certifications for ISO 9001 and 13485, Health Canada Class II, and CE Mark (EU) and prepared for/initiated FDA approval, DoD Information Assurance Ann Unitas, PMP 703-***-**** ***.******@*****.*** Certification and Accreditation ... - 2019 Jun 10
MD. MHA
Silver Spring, MD, 20910
... Iran Advised Post-Marketing Surveillance of cosmetic products and cooperated with Iranian Food & Drug Administration (FDA) Investigated staff based on FDA protocols and regulation updates for proper safety procedures in labeling the products, ... - 2019 May 30
... Iran Advised Post-Marketing Surveillance of cosmetic products and cooperated with Iranian Food & Drug Administration (FDA) Investigated staff based on FDA protocols and regulation updates for proper safety procedures in labeling the products, ... - 2019 May 30
Chief Information Officer
McLean, VA
... Automated, consolidated and standardized data collection on web portal for FDA approval, using blended internal and outsourced resources for follow-the-sun development. GMAC Commercial Mortgage, Horsham, PA 1999 to 2006 Formerly part of General ... - 2019 Apr 27
... Automated, consolidated and standardized data collection on web portal for FDA approval, using blended internal and outsourced resources for follow-the-sun development. GMAC Commercial Mortgage, Horsham, PA 1999 to 2006 Formerly part of General ... - 2019 Apr 27
Data Analyst Project Manager
Sterling, VA, 20164
... Research Assistant Point of Care Technologies, Inc, Rockville, MD, Jul 97-Dec 99 Assist in preparation and studies for 510(K) pre-market notification application to FDA for Fingerprint Drug Screening DeviceTM and Genie CupTM to include: cross ... - 2019 Apr 23
... Research Assistant Point of Care Technologies, Inc, Rockville, MD, Jul 97-Dec 99 Assist in preparation and studies for 510(K) pre-market notification application to FDA for Fingerprint Drug Screening DeviceTM and Genie CupTM to include: cross ... - 2019 Apr 23
Pilot Technician
Upper Marlboro, MD
... Project, Outlook, Word, Excel, and Access cGMP/cGLP environment and guidelines with chemical and biological sciences FDA regulations and reporting policies Electronic Medical Records (EMR) Scientific data abstraction Product Development and ... - 2019 Apr 22
... Project, Outlook, Word, Excel, and Access cGMP/cGLP environment and guidelines with chemical and biological sciences FDA regulations and reporting policies Electronic Medical Records (EMR) Scientific data abstraction Product Development and ... - 2019 Apr 22
Clinical Research Data Entry
Hyattsville, MD
... Capture platform CLINICAL RESEARCH TRAINING GCPs/ICH Guidelines CAPA Fraud and Misconducts NIH Protecting Human Research Subjects FDA Guidelines (21CFR Parts 50,54,56,312) HIPAA Regulations Monitoring Guidelines and Procedures Regulatory Documents – ... - 2019 Apr 15
... Capture platform CLINICAL RESEARCH TRAINING GCPs/ICH Guidelines CAPA Fraud and Misconducts NIH Protecting Human Research Subjects FDA Guidelines (21CFR Parts 50,54,56,312) HIPAA Regulations Monitoring Guidelines and Procedures Regulatory Documents – ... - 2019 Apr 15
Accounting Accountant
Washington, DC
... Staff Accountant Generating multiple invoices to government departments including DoD, FDA, SSA, SBA, etc. via government websites or systems monthly. Providing full cycle accounting works, Payroll entry, financial reports analyze. Providing support ... - 2019 Apr 09
... Staff Accountant Generating multiple invoices to government departments including DoD, FDA, SSA, SBA, etc. via government websites or systems monthly. Providing full cycle accounting works, Payroll entry, financial reports analyze. Providing support ... - 2019 Apr 09
QA Lead
Chantilly, VA
... Client: Food and Drug Administration, White Oak, MD Role: Quality Assurance Lead, Project: eSubmitter Dec 2010 to July 2012 FDA receives product and company registrations from various pharmaceutical companies, currently the process is manual and ... - 2019 Mar 11
... Client: Food and Drug Administration, White Oak, MD Role: Quality Assurance Lead, Project: eSubmitter Dec 2010 to July 2012 FDA receives product and company registrations from various pharmaceutical companies, currently the process is manual and ... - 2019 Mar 11
Sas Manager
Woodbridge, VA
... Bristol-Myers Squibb (BMS), New Brunswick, NJ, 11/02 to 01/04 Principal Implementer Designed & developed of a comprehensive statistical system for the à oAnalysis of drug stability oPrediction of release estimates consistent with FDA 21 CFR par 11 ... - 2019 Mar 10
... Bristol-Myers Squibb (BMS), New Brunswick, NJ, 11/02 to 01/04 Principal Implementer Designed & developed of a comprehensive statistical system for the à oAnalysis of drug stability oPrediction of release estimates consistent with FDA 21 CFR par 11 ... - 2019 Mar 10
Sales Clinical Research
Silver Spring, MD
... Started career at Buc & Beardsely, a law firm specializing in FDA/healthcare matters. Education: Received a Juris Doctorate from the Syracuse University School of Law and a BS degree in Public Relations and Marketing from the SI Newhouse School of ... - 2019 Mar 09
... Started career at Buc & Beardsely, a law firm specializing in FDA/healthcare matters. Education: Received a Juris Doctorate from the Syracuse University School of Law and a BS degree in Public Relations and Marketing from the SI Newhouse School of ... - 2019 Mar 09