| Resume alert | Resumes 21 - 30 of 24045 |
Mental Health Case Management
Greensburg, PA
... Program design Care plans SharePoint Supervising experience Clinical trials Crisis intervention EMR systems Microsoft Excel FDA regulations Teaching PTSD Care Microsoft Word Sports coaching Administrative experience Child & family counseling Social ... - Apr 16
... Program design Care plans SharePoint Supervising experience Clinical trials Crisis intervention EMR systems Microsoft Excel FDA regulations Teaching PTSD Care Microsoft Word Sports coaching Administrative experience Child & family counseling Social ... - Apr 16
Development Operations Clinical
Jersey City, NJ
... Skilled in leading cross-functional product development programs and Clinical trial team management, specifically developing and implementing strategic product development plans, and ensuring compliance with FDA regulations and ICH guidelines. ... - Apr 16
... Skilled in leading cross-functional product development programs and Clinical trial team management, specifically developing and implementing strategic product development plans, and ensuring compliance with FDA regulations and ICH guidelines. ... - Apr 16
Site Safety High Tech
Phoenix, AZ
... Hazardous Waste management, ventilation/hood Air Quality management, General Hazard Awareness, Warehouse/Dock safety, power washing, Sanitizing/Disinfecting, Food Processing plant safety, Maintenance, USDA,FDA compliance and client relations. ... - Apr 16
... Hazardous Waste management, ventilation/hood Air Quality management, General Hazard Awareness, Warehouse/Dock safety, power washing, Sanitizing/Disinfecting, Food Processing plant safety, Maintenance, USDA,FDA compliance and client relations. ... - Apr 16
Security Guard High School
Warren, MI
... • SAP • Analysis skills • Adobe Creative Suite • Leadership • ERP systems • Manufacturing & utilities (3 years) • CGMP • FDA regulations • Bookkeeping • Management • Heavy lifting • Warehouse management system • AS400 • Warehouse distribution • ... - Apr 16
... • SAP • Analysis skills • Adobe Creative Suite • Leadership • ERP systems • Manufacturing & utilities (3 years) • CGMP • FDA regulations • Bookkeeping • Management • Heavy lifting • Warehouse management system • AS400 • Warehouse distribution • ... - Apr 16
Document Control Specialist
Milpitas, CA
... Sunnyvale CA Document Controller/ CAPA Coordinator – Issue, process and implement NOC (Notice of Change) for FDA regulated Medical Products. Assist originators with assessing levels of changes, the corresponding attachments that apply, and creating ... - Apr 16
... Sunnyvale CA Document Controller/ CAPA Coordinator – Issue, process and implement NOC (Notice of Change) for FDA regulated Medical Products. Assist originators with assessing levels of changes, the corresponding attachments that apply, and creating ... - Apr 16
Quality Engineer Assurance
Livonia, MI
... Completed FDA-QSR registration and compliance to 21CFR820. Initiated cross-functional Material Review Board process. Improved throughput and hold timing of nonconforming material. Acted as interim Account Manager to support 4 key accounts while new ... - Apr 16
... Completed FDA-QSR registration and compliance to 21CFR820. Initiated cross-functional Material Review Board process. Improved throughput and hold timing of nonconforming material. Acted as interim Account Manager to support 4 key accounts while new ... - Apr 16
Quality Assurance Medical Devices
Manhattan, NY, 10019
... Follow FDA, TUK- SUD AND ISO guidelines for build and test Medical Devices. Testing and fixing trouble shooting in Sub Assy. Refurbishing Instruments. Samblasting machine Sand blending, polsishing in to the machine shop Cycle Count with SAP System. ... - Apr 16
... Follow FDA, TUK- SUD AND ISO guidelines for build and test Medical Devices. Testing and fixing trouble shooting in Sub Assy. Refurbishing Instruments. Samblasting machine Sand blending, polsishing in to the machine shop Cycle Count with SAP System. ... - Apr 16
Clinical Trials Trial
Temecula, CA
... administrative functions to ensure relevant process are performed in accordance with the Code of Federal Regulations (CFR) of the Food and Drug Administration (FDA) and the International Conference on Harmonization/Good Clinical Practice (ICH-GCP). ... - Apr 15
... administrative functions to ensure relevant process are performed in accordance with the Code of Federal Regulations (CFR) of the Food and Drug Administration (FDA) and the International Conference on Harmonization/Good Clinical Practice (ICH-GCP). ... - Apr 15
Scrum Master Product Manager
The Hammocks, FL, 33186
... • Supported development teams in interpreting and implementing regulatory guidelines including cGMP, ISO standards, and FDA regulations; helped align development processes and documentation to meet quality and compliance standards. • Consistently ... - Apr 15
... • Supported development teams in interpreting and implementing regulatory guidelines including cGMP, ISO standards, and FDA regulations; helped align development processes and documentation to meet quality and compliance standards. • Consistently ... - Apr 15
Clinical Research Trial
Baltimore, MD
... Clinical Research Coordinator, FyMed, Inc., Wilmington, DE 2012 – 2015 Provided viable support to staff in coordination of clinical research projects and ensured compliance with regulatory standards, including FDA regulations and Institutional ... - Apr 15
... Clinical Research Coordinator, FyMed, Inc., Wilmington, DE 2012 – 2015 Provided viable support to staff in coordination of clinical research projects and ensured compliance with regulatory standards, including FDA regulations and Institutional ... - Apr 15