Full-Time
Confirmed live in the last 24 hours
$28 - $31Hourly
Entry, Junior
Broomfield, CO, USA
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Company Size
1,001-5,000
Company Stage
Acquired
Total Funding
N/A
Headquarters
null
Founded
1980
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Casual Work Environment
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Zoll Medical Corp. is asking a Boston federal judge to toss a proposed class action brought by medical device customers whose personal information was released during a ransomware attack last year...
CHELMSFORD, Mass.--(BUSINESS WIRE)--ZOLL®, an Asahi Kasei company that manufactures medical devices and related software solutions, announced today that it has received an Innovative Technology contract from Vizient, Inc., the nation’s largest provider-driven healthcare performance improvement company. The contract was awarded based on the recommendation of hospital experts who serve on one of Vizient’s customer-led councils, and it signifies unique qualities that potentially bring improvement to patient cardiovascular care. Innovative Technology contracts are recommended after review and interaction with products submitted through Vizient’s Innovative Technology Program. Vizient customer-led councils identify technologies that have the potential to enhance clinical care, patient safety, healthcare worker safety, or improve business operations of healthcare organizations. “Each year, more than 258,000 patients in the U.S. access emergency rooms as a result of heart attacks,1” said Matt Rochner, TherOx General Manager
CHELMSFORD, Mass.--(BUSINESS WIRE)--ZOLL®, spółka z Grupy Asahi Kasei produkująca wyroby medyczne i powiązane oprogramowanie, ogłosiła dzisiaj, że defibrylator ZOLL AED 3® został zatwierdzony zgodnie z unijnym rozporządzeniem (UE) 2017/745 w sprawie wyrobów medycznych, zwanym w skrócie „EU MDR”. EU MDR to wprowadzone przez Unię Europejską rozporządzenie 2017/745 w sprawie wyrobów medycznych przyjęte przez Parlament Europejski i Radę w 2017 r. Celem EU MDR jest zagwarantowanie wysokich standardów bezpieczeństwa i jakości wyrobów medycznych wytwarzanych w państwach członkowskich Unii Europejskiej lub dostarczanych na ich terytorium. Firma ZOLL uzyskała właśnie oznakowanie CE swojego defibrylatora ZOLL AED 3 zgodnie z przepisami EU MDR
CHELMSFORD, Massachusetts--(BUSINESS WIRE)--ZOLL®, una società di Asahi Kasei che produce dispositivi medici e soluzioni software correlate, ha annunciato oggi che il defibrillatore ZOLL AED 3® ha ricevuto l'approvazione ai sensi del regolamento UE 2017/745 relativo ai dispositivi medici, noto comunemente come MDR UE. Il regolamento MDR UE è il regolamento europeo in materia di dispositivi medici 2017/745 proposto nel 2017 dal Parlamento europeo e dal Consiglio dell'Unione europea. Lo scopo del MDR UE è di garantire un elevato standard di sicurezza e qualità per i dispositivi medici prodotti o forniti all'interno dei paesi membri dell'Unione europea. ZOLL ha ottenuto la marcatura CE per il suo defibrillatore ZOLL AED 3 ai sensi del regolamento MDR UE