| Resume alert | Resumes 11 - 20 of 352 |
Quality Assurance Data Management
Philadelphia, PA
... provided Quality oversight of internal and external clinical trial activities, related records, and processes to assure management in accordance with FDA regulations, ICH-GCP, SOPs and all other applicable regulations and assisted with other tasks ... - Feb 26
... provided Quality oversight of internal and external clinical trial activities, related records, and processes to assure management in accordance with FDA regulations, ICH-GCP, SOPs and all other applicable regulations and assisted with other tasks ... - Feb 26
Business Development Technical Support
Havertown, PA
... ability to talk with individuals at all levels • Very knowledgeable with CRO, Clinical trial processes, HIPAA and other myriad FDA regulations and compliances Professional Experience Diagnostic Solutions Laboratory 2013-2022 Director, New Business ... - Feb 22
... ability to talk with individuals at all levels • Very knowledgeable with CRO, Clinical trial processes, HIPAA and other myriad FDA regulations and compliances Professional Experience Diagnostic Solutions Laboratory 2013-2022 Director, New Business ... - Feb 22
Analytical, great communicator, strategic, planning & organized
Pennsauken, NJ
... lung, and gastric cancers across 15 sites in the United States from start-up activities including feasibility, final protocol, FDA follow-up, study and site contracts and budgets, master ICF development and approval, oversight of site ICF ... - Feb 18
... lung, and gastric cancers across 15 sites in the United States from start-up activities including feasibility, final protocol, FDA follow-up, study and site contracts and budgets, master ICF development and approval, oversight of site ICF ... - Feb 18
Data Entry Quality Control
New Castle, DE
... and in compliance with federal and state regulations and guidelines including FDA, EPA, DOT, OSHA, & DEA Ensures accurate, up-to-date records of inventory through SAP and daily operations, completes necessary forms and data entry is completed. ... - Feb 14
... and in compliance with federal and state regulations and guidelines including FDA, EPA, DOT, OSHA, & DEA Ensures accurate, up-to-date records of inventory through SAP and daily operations, completes necessary forms and data entry is completed. ... - Feb 14
Business Development Revenue Growth
Philadelphia, PA
... Key Achievements: • Secured FDA approval for five items within a 24-month timeframe. • Introduced high-speed, needle-free injection systems at US military bases. • Positioned the company as a frontrunner in global health endeavors targeting ... - Feb 11
... Key Achievements: • Secured FDA approval for five items within a 24-month timeframe. • Introduced high-speed, needle-free injection systems at US military bases. • Positioned the company as a frontrunner in global health endeavors targeting ... - Feb 11
Phlebotomist
Philadelphia, PA
... Knowledge of FDA and HIPPA regulations, medical terminology, laboratory testing procedures and equipment. Familiar with GLP and GCP environment. A highly motivated person with strong analytical and organizational skills. A dedicated team player also ... - Feb 06
... Knowledge of FDA and HIPPA regulations, medical terminology, laboratory testing procedures and equipment. Familiar with GLP and GCP environment. A highly motivated person with strong analytical and organizational skills. A dedicated team player also ... - Feb 06
Shift Supervisor
Philadelphia, PA
... Comply to all SOP, cGMP, SAP, AND FDA standards. October 2004- March 2018 Animas Corporation of Johnson & Johnson West Chester, PA Served in several employment capacities and have demonstrated Johnson & Johnson Credo values while fulfilling numerous ... - Feb 05
... Comply to all SOP, cGMP, SAP, AND FDA standards. October 2004- March 2018 Animas Corporation of Johnson & Johnson West Chester, PA Served in several employment capacities and have demonstrated Johnson & Johnson Credo values while fulfilling numerous ... - Feb 05
R D Product Development
Garnet Valley, PA
... Creator and Chairperson of Committee for Product Development, technical transfer to submission, validation and product launch resulting in optimal communication, accountability, flow, timely submissions and product launch per FDA approval schedule. ... - Jan 11
... Creator and Chairperson of Committee for Product Development, technical transfer to submission, validation and product launch resulting in optimal communication, accountability, flow, timely submissions and product launch per FDA approval schedule. ... - Jan 11
Social Media Information Technology
Philadelphia, PA
... (1997-1999) AstraZeneca FDA regulation compliance Implement ISO best practices/processes Education Master’s Degree (MA) Columbia University NYC NY Biochemistry/Education Bachelor’s Degree (BA) University of Pennsylvania Philadelphia, PA Biochemistry ... - Jan 10
... (1997-1999) AstraZeneca FDA regulation compliance Implement ISO best practices/processes Education Master’s Degree (MA) Columbia University NYC NY Biochemistry/Education Bachelor’s Degree (BA) University of Pennsylvania Philadelphia, PA Biochemistry ... - Jan 10
Regulatory Affairs Compliance Specialist
Vineland, NJ
... Strong working knowledge of FDA and USDA regulations and cGMP’s. Experienced in FDA regulated electronic submissions, with emphasis on CMC. Experienced proofreader. Experienced in Microsoft Word, Excel, Access, Power Point, Zetadocs and Abode. ... - Jan 10
... Strong working knowledge of FDA and USDA regulations and cGMP’s. Experienced in FDA regulated electronic submissions, with emphasis on CMC. Experienced proofreader. Experienced in Microsoft Word, Excel, Access, Power Point, Zetadocs and Abode. ... - Jan 10