| Resume alert | Resumes 31 - 40 of 24101 |
Project Manager Management
Rougemont, NC
... Her major accomplishments are FDA/EMEA IND approvals, Six Sigma yellow belt project to save $183K, and dissecting supply chain to save over $600K. Professional Experience Jun 2022- Dec 2023 Sun Pharma contract opportunity/ Princeton, NJ Sr Clinical ... - Apr 30
... Her major accomplishments are FDA/EMEA IND approvals, Six Sigma yellow belt project to save $183K, and dissecting supply chain to save over $600K. Professional Experience Jun 2022- Dec 2023 Sun Pharma contract opportunity/ Princeton, NJ Sr Clinical ... - Apr 30
Case Management
Raleigh, NC
... Prior Authorization Processes, and Switching Infusion Sites as well as Healthcare Providers Reporting and Complying with FDA for Adverse Events and product Complaints, while Educating Patients on Processes of Replacement Doses Working with Biogen ... - Apr 30
... Prior Authorization Processes, and Switching Infusion Sites as well as Healthcare Providers Reporting and Complying with FDA for Adverse Events and product Complaints, while Educating Patients on Processes of Replacement Doses Working with Biogen ... - Apr 30
Data Analyst Power Bi
Godfrey, IL
... biochemistry industries Skilled in database design, data cleansing, and compliance with regulatory standards like HIPAA and FDA Strong track record of completing ad hoc queries, automating data loading, and ensuring data integrity for impactful data ... - Apr 30
... biochemistry industries Skilled in database design, data cleansing, and compliance with regulatory standards like HIPAA and FDA Strong track record of completing ad hoc queries, automating data loading, and ensuring data integrity for impactful data ... - Apr 30
Clinical Research Associate
Plano, TX
... Health Data Analytics GCP/ICH Guidelines Data Management Health Information Systems FDA Regulatory Requirements COMPUTER SKILLS: Windows XP, Microsoft Word, PowerPoint, Excel, Access, CTMS, EDC(Medidata Rave, Inform, Phase Forward), Salesforce, TMF. ... - Apr 30
... Health Data Analytics GCP/ICH Guidelines Data Management Health Information Systems FDA Regulatory Requirements COMPUTER SKILLS: Windows XP, Microsoft Word, PowerPoint, Excel, Access, CTMS, EDC(Medidata Rave, Inform, Phase Forward), Salesforce, TMF. ... - Apr 30
Sales Manager Advertising
Anaheim, CA
... The co tried to get FDA approval and the got shut them down as Dr’s were only able to use the machine, so company closed. Auto one Warranty: Dec 7 2006- May 15,2010 I sold people who called in to provide them and extended warranty when their current ... - Apr 29
... The co tried to get FDA approval and the got shut them down as Dr’s were only able to use the machine, so company closed. Auto one Warranty: Dec 7 2006- May 15,2010 I sold people who called in to provide them and extended warranty when their current ... - Apr 29
Business Management International
La Jolla, CA
... Applied continuous pressure to quality assurance FDA mandates, currently to two non-conforming production lot receipts and from additional past remediation effort issue discretions which resulted in the supplier issuing our company $111,000+ in a ... - Apr 29
... Applied continuous pressure to quality assurance FDA mandates, currently to two non-conforming production lot receipts and from additional past remediation effort issue discretions which resulted in the supplier issuing our company $111,000+ in a ... - Apr 29
Field Service Project Management
Arizona
... Follow and adhere to ISO, GMP and FDA regulations and requirements. Address all levels of customer needs, chemistry, instrumentation, software and computer. Responsible for the state of Arizona and Las Vegas, NV. as a single source support engineer. ... - Apr 29
... Follow and adhere to ISO, GMP and FDA regulations and requirements. Address all levels of customer needs, chemistry, instrumentation, software and computer. Responsible for the state of Arizona and Las Vegas, NV. as a single source support engineer. ... - Apr 29
Medical Devices Production Manager
Hollywood, FL
... Knowledge in FDA–regulated manufacturing operations Class III and Class VIII medical devices, with extensive understanding of GMP, and GDP methodologies. Areas of Competence oLeadership/Owner Ship oSupervisory/Management oCommunication Skills oNew ... - Apr 29
... Knowledge in FDA–regulated manufacturing operations Class III and Class VIII medical devices, with extensive understanding of GMP, and GDP methodologies. Areas of Competence oLeadership/Owner Ship oSupervisory/Management oCommunication Skills oNew ... - Apr 29
Co-founder, Project and Operations Manager, Business Development, PMP
Chicago, IL
... Al YAS Gate, Dubai, UAE Business Development Engineer (Medical Devices) October 2011 – December 2012 Researched, Strategized and Marketed an FDA cleared Class II medical device Air Disinfection System to Hospitals and Healthcare professionals. ... - Apr 29
... Al YAS Gate, Dubai, UAE Business Development Engineer (Medical Devices) October 2011 – December 2012 Researched, Strategized and Marketed an FDA cleared Class II medical device Air Disinfection System to Hospitals and Healthcare professionals. ... - Apr 29
Quality Assurance Regulatory Affairs
Kendall Park, NJ
... EDUCATION Master’s of Science in Regulatory Affairs & Health Policy MCPHS University Boston, MA Dec 2017 GPA:3.91/4.00 Bachelor’s of Science in Pharmacy Veer Narmad South Gujarat University India May 2005 GPA: 3.25/4.00 EDUCATION DETAILS • FDA ... - Apr 29
... EDUCATION Master’s of Science in Regulatory Affairs & Health Policy MCPHS University Boston, MA Dec 2017 GPA:3.91/4.00 Bachelor’s of Science in Pharmacy Veer Narmad South Gujarat University India May 2005 GPA: 3.25/4.00 EDUCATION DETAILS • FDA ... - Apr 29