| Resume alert | Resumes 81 - 90 of 24662 |
Business Development Product Management
Newark, DE
... payers, associations, and the Medical Imaging and Technology Alliance (MITA) to develop AI-driven best practices requirements for FDA submission of AI-based technology ●Contributing member of Varian acquisition team aligning AI solutions to Varian’s ... - Sep 13
... payers, associations, and the Medical Imaging and Technology Alliance (MITA) to develop AI-driven best practices requirements for FDA submission of AI-based technology ●Contributing member of Varian acquisition team aligning AI solutions to Varian’s ... - Sep 13
Clinical Research Associate
Dunedin, FL
... Summary of experience: Accomplished Clinical Research Associate with 19 years' experience in the industry with working knowledge of drug development process, FDA regulatory requirements, Good Clinical Practices, ICH guidelines and HIPAA regulations. ... - Sep 13
... Summary of experience: Accomplished Clinical Research Associate with 19 years' experience in the industry with working knowledge of drug development process, FDA regulatory requirements, Good Clinical Practices, ICH guidelines and HIPAA regulations. ... - Sep 13
Human Resource Shipping Supervisor
DeSoto, TX
... ·Perform freight handling using appropriate motorized and manual equipment, including but not limited to: forklift, pallet jack and hand truck ·Working knowledge of OSHA, DOT, HAZMAT, FDA regulations ·Supervise the daily activities of the warehouse. ... - Sep 13
... ·Perform freight handling using appropriate motorized and manual equipment, including but not limited to: forklift, pallet jack and hand truck ·Working knowledge of OSHA, DOT, HAZMAT, FDA regulations ·Supervise the daily activities of the warehouse. ... - Sep 13
Ux Designer Ui
San Jose, CA
... • Demonstrated experience in the medical product industry with a strong understanding of IEC 62366-1 and FDA Human Factors Guidance. Proficient in IEC 62304 (software lifecycle processes for medical devices), ensuring compliance and usability in ... - Sep 13
... • Demonstrated experience in the medical product industry with a strong understanding of IEC 62366-1 and FDA Human Factors Guidance. Proficient in IEC 62304 (software lifecycle processes for medical devices), ensuring compliance and usability in ... - Sep 13
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 ... - Sep 13
... 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 ... - Sep 13
Customer Service Experience
McKeesport, PA
... employees on food preparation, sanitation procedures according to OSHA requirements, and other McDonald's mandated procedures or FDA provisions• Maintained detailed descriptions for food Inventory as well as overall appearance• Prepared reports ... - Sep 13
... employees on food preparation, sanitation procedures according to OSHA requirements, and other McDonald's mandated procedures or FDA provisions• Maintained detailed descriptions for food Inventory as well as overall appearance• Prepared reports ... - Sep 13
Data Entry Customer Service
Anderson, IN, 46016
... (FDA Data Entry) – Inputting studies for the FDA. Data entry of clinical data provided by written case report forms or case report form images. Tracking of case reports forms and other clinical documents upon receipt. Assisting quality control of ... - Sep 12
... (FDA Data Entry) – Inputting studies for the FDA. Data entry of clinical data provided by written case report forms or case report form images. Tracking of case reports forms and other clinical documents upon receipt. Assisting quality control of ... - Sep 12
Lean Six Sigma, Secret Clearance
Signal Hill, CA, 90755
... P&L of $400 Mil to $4.0 Billion for multi-site and country operations with up to 4,000 employees in automotive, high-tech manufacturing of consumer and commercial electronics, avionics, airframe, defense, FDA, industrial and E&I with a DOD Secret ... - Sep 12
... P&L of $400 Mil to $4.0 Billion for multi-site and country operations with up to 4,000 employees in automotive, high-tech manufacturing of consumer and commercial electronics, avionics, airframe, defense, FDA, industrial and E&I with a DOD Secret ... - Sep 12
Analytical Chemist Product Testing
Suffern, NY
... for GC/MS Analysis ●Derivatization of drug ●Analysis of specimen using GC/MS ABEY VARGHESE Page 2 BARR PHARMACEUTICALS (Teva), Pomona, NY 2006-2009 Research Chemist A Generic Pharmaceutical Company working in a FDA Regulated GMP Environment. ... - Sep 12
... for GC/MS Analysis ●Derivatization of drug ●Analysis of specimen using GC/MS ABEY VARGHESE Page 2 BARR PHARMACEUTICALS (Teva), Pomona, NY 2006-2009 Research Chemist A Generic Pharmaceutical Company working in a FDA Regulated GMP Environment. ... - Sep 12
Warehouse Associate Team Lead
Allentown, PA
... • Outpatient • Live-in employment • Home care • Home health • Long term care • Home & community care • Assembly • Quality control • FDA regulations • Manufacturing • CGMP • Computer skills • Packaging • Hazardous material identification • Restaurant ... - Sep 12
... • Outpatient • Live-in employment • Home care • Home health • Long term care • Home & community care • Assembly • Quality control • FDA regulations • Manufacturing • CGMP • Computer skills • Packaging • Hazardous material identification • Restaurant ... - Sep 12