| Distance: | Resume alert | Resumes 1 - 10 of 634 |
Quality Assurance Research Associate/ Clinical Trial Associate
Washington, DC
... Research Associate/Quality Control Oversight - Controlled Human Malaria Infection § Quality Assurance Lead - SOP compliance, procedure documentation, COA tracking § Trial Master File - FDA regulations, quality assurance tracking and documentation. ... - Jul 02
... Research Associate/Quality Control Oversight - Controlled Human Malaria Infection § Quality Assurance Lead - SOP compliance, procedure documentation, COA tracking § Trial Master File - FDA regulations, quality assurance tracking and documentation. ... - Jul 02
Clinical Research Patient Care
Washington, DC
... FDA Focus) (CITI Program, Online) (Aug. 06, 2024) Research With Minors - BIOMED (CITI Program, Online) (Aug. 06, 2024) FDA-Regulated Research (CITI Program, Online) (Aug. 05, 2024) The Professional Medical Interpreter® (Academy of Interpretation, ... - Jun 27
... FDA Focus) (CITI Program, Online) (Aug. 06, 2024) Research With Minors - BIOMED (CITI Program, Online) (Aug. 06, 2024) FDA-Regulated Research (CITI Program, Online) (Aug. 05, 2024) The Professional Medical Interpreter® (Academy of Interpretation, ... - Jun 27
Clinical Testing Manager
Washington, DC, 20017
... **** **** ****** ** Washington DC 20017 Email: *********@*****.*** Phone: 304-***-**** Summary Extensive work experience in GCLP, GLP, GMP and FDA regulated laboratories 19 years of laboratory experience, including in-house developed ELISAs, ... - Jun 25
... **** **** ****** ** Washington DC 20017 Email: *********@*****.*** Phone: 304-***-**** Summary Extensive work experience in GCLP, GLP, GMP and FDA regulated laboratories 19 years of laboratory experience, including in-house developed ELISAs, ... - Jun 25
D C Law Enforcement
Silver Spring, MD
... FDA. Prepare exhibits for summary judgment and pre-trial motions. Depo Digest. Document review on Concordance. Create Witness binders. Redline document. Track docket activity on cases. Department of Justice, Antitrust & Civil Divisions, Washington, ... - Jun 19
... FDA. Prepare exhibits for summary judgment and pre-trial motions. Depo Digest. Document review on Concordance. Create Witness binders. Redline document. Track docket activity on cases. Department of Justice, Antitrust & Civil Divisions, Washington, ... - Jun 19
North America Business Leadership
Washington, DC, 20003
CAREER SUMMARY • Neurotech leader with **+ years of experience applying neuroscientific training with business leadership skills to create a winning strategy, team, and awareness to scale over 50 FDA-cleared products and platforms to market, ... - Jun 14
CAREER SUMMARY • Neurotech leader with **+ years of experience applying neuroscientific training with business leadership skills to create a winning strategy, team, and awareness to scale over 50 FDA-cleared products and platforms to market, ... - Jun 14
Project Management Power Bi
Rockville, MD
... Fagron Sterile Services – Wichita, KS Quality Control Specialist February 2016 – December 2018 Performed 100+ bioburden and endotoxin tests per batch, ensuring compliance with FDA regulations (21 CFR 210/211) and optimizing testing protocols. Led 30 ... - Jun 09
... Fagron Sterile Services – Wichita, KS Quality Control Specialist February 2016 – December 2018 Performed 100+ bioburden and endotoxin tests per batch, ensuring compliance with FDA regulations (21 CFR 210/211) and optimizing testing protocols. Led 30 ... - Jun 09
Sr Principal Enterprise Architect
Ashburn, VA
... readiness for Oracle RDBMS 19c & Oracle 12 EBS platforms o UFMS platform mixed systems application interfaces (PSC, FDA, CDC, IHS) batch processing o Consolidated operational data reporting platforms (Informatica data management/analytics) o ... - Jun 08
... readiness for Oracle RDBMS 19c & Oracle 12 EBS platforms o UFMS platform mixed systems application interfaces (PSC, FDA, CDC, IHS) batch processing o Consolidated operational data reporting platforms (Informatica data management/analytics) o ... - Jun 08
Healthcare Quality Information Systems
Oakton, VA
... user training, application overview and address help desk issues ● Executed test validations at various levels including database validation, UI validation and UAT validation to meet the yearly regulatory FDA compliance and other regulatory audits. ... - Jun 07
... user training, application overview and address help desk issues ● Executed test validations at various levels including database validation, UI validation and UAT validation to meet the yearly regulatory FDA compliance and other regulatory audits. ... - Jun 07
Medical device Quality Engineer
Takoma Park, MD
... in all aspects of Quality functions & Risk Management, supporting design engineering/design control development, implementation, and remediation of Class II and Class III devices in compliance with FDA & international (ISO 13485) device regulations. ... - Jun 06
... in all aspects of Quality functions & Risk Management, supporting design engineering/design control development, implementation, and remediation of Class II and Class III devices in compliance with FDA & international (ISO 13485) device regulations. ... - Jun 06
Automation Engineer Qa Analyst
Dumfries, VA
... FDA (U.S. Department of Health & Human Services), Arlington, VA Test Automation Engineer Jan, 2017 – July, 2017 Responsibilities: oSoftware Test Automation Engineer/QA Analyst with expertise in writing Test Plan/ Test Cases, design Automation Test ... - Jun 05
... FDA (U.S. Department of Health & Human Services), Arlington, VA Test Automation Engineer Jan, 2017 – July, 2017 Responsibilities: oSoftware Test Automation Engineer/QA Analyst with expertise in writing Test Plan/ Test Cases, design Automation Test ... - Jun 05