Will need to provide the required in-service education to customers.
Responsible for ensuring the proper technical scope review has been conducted prior to sale.
Must maintaining organized account records, including account profiles and maintaining those in the company CRM Salesforce.com.
Responsible for providing various reports as required by management. These shall include, but are not limited to, weekly expense reports, monthly and quarterly forecasts, and regular up-to-date activity reporting.
Expectation for maintaining and tracking demo and evaluation inventory and documenting the use there of in Salesforce.com. In addition, equipment must be maintained and presented in good working manner.
Spend a minimum of 3 days per week working in the field
Other projects as assigned
Required/Preferred Education and Experience
Knowledge, Skills and Abilities
Physical Demands
Salary for this position is $60,000 ($175,000 OTE) annually. Final compensation will be determined by various factors such as a candidate’s relevant work experience, skills, certifications, and location.
ZOLL is a fast-growing company that operates in more than 140 countries around the world. Our employees are inspired by a commitment to make a difference in patients's lives, and our culture values innovation, self-motivation and an entrepreneurial spirit. Join us in our efforts to improve outcomes for underserved patients suffering from critical cardiopulmonary conditions and help save more lives.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
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$60k - $175k/yr
Mid, Senior
Akron, OH, USA + 2 more
More locations: Cleveland, OH, USA | Canton, OH, USA
Candidates must live in the Cleveland, Akron, Canton, Ohio territory.
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Company Size
1,001-5,000
Company Stage
Acquired
Total Funding
$2.2B
Headquarters
null
Founded
1980
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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