ENDOLOGIX INC

Endologix, Inc. develops, manufactures, markets, and sells medical devices for the treatment of abdominal aortic aneurysms in the United States and internationally. The company offers minimally-invasive endovascular aneurysm repair (EVAR), including AFX (Anatomical Fixation) endovascular AAA system, which is a minimally invasive delivery system; VELA Proximal Endograft, which is designed for the treatment of proximal aortic neck anatomies with AFX; and the Ovation abdominal stent graft system. It also provides endovascular aneurysm sealing system (EVAS) product that is based on the Nellix EVAS ... system to seal the aneurysm, and provides blood flow to the legs through two blood lumens. In addition, the company offers proximal aortic extensions and limb extensions, which allow physicians to customize the implant to fit the patient's anatomy; and accessories to facilitate the delivery of its EVAR and EVAS products, including compatible guidewires, inflation devices, and snares. It sells its products through direct sales force, and a network of third party distributors and agents. The company was formerly known as Radiance Medical Systems, Inc. and changed its name to Endologix, Inc. in May 2002. Endologix, Inc. was founded in 1992 and is headquartered in Irvine, California. More

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Overview. Endologix develops and manufactures minimally invasive treatments for aortic disorders. We offer a dynamic, growth environment, competitive compensation and benefits, and a challenging, fulfilling experience in a fast-paced, growing company. Medical device professionals have the opportunity to develop and further their careers in a dynamic company that features the latest innovations in endovascular aneurysm repair and sealing. Job Scope:. The Endologix Clinical Specialist supports the sales efforts and enhances the productivity of the Endologix sales team by providing implanting cus... view job details

Overview. This position provides communication and follow-up to customer and sales representatives regarding the analysis results of customer complaints for Endologix products.  The incumbent will evaluate incoming information, and evaluate the relationship between the product and any clinical event, and communicates event investigation via regulatory reports within required timelines. This process is governed by FDA Quality System Regulations (QSR), ISO 13485:2033, Good Manufacturing Practices (GMPs), Medical Device Directive, Canadian, JPAL and international regulatory requirements.. Respons... view job details

Overview:. The Global Product Manager will be responsible for the commercial launch of ALTO in OUS regions (Japan, EU, Canada, LATAM, APAC) and managing a sustaining product, AFX2, globally while working closely with US and OUS product marketing counterparts to achieve global commercial launch excellence. Strong collaboration and leadership skills is key to effectively work with sales and marketing counterparts. Will develop in-depth knowledge of EVAR, and abdominal aortic aneurysm disease state (AAA), company products & customers. High degree of clinical & product knowledge will be required, ... view job details

Overview. Team Leader responsible for providing leadership and supervision for Machine Shop and prioritize activities required to meet production, quality, and safety objectives. Will oversee and machine complex prototype tooling components with CNC and manual machines as well as with imported CAD models to develop programs for lathe, vertical, and multi-axis CNC machining centers. Will work with ultra-close tolerances in a fast paced in-house shop environment. Works closely with Director/Manager, Operations Engineering, and interfaces with cross-functional technical groups such as R&D, MEPD a... view job details

Overview. Researches, writes and edits regulatory procedures and technical documents. Summarizes data from bench, nonclinical, clinical studies, post-market surveillance, and manufacturing process qualifications. Prepares documents that may be submitted to the US Food and Drug Administration (FDA) and other Global Health Authorities; these documents may be further used for scientific publication, peer-to-peer or lay person communications and/or presentations. Develops and edits content for scientific manuscripts and presentations. Assists in the development of document standards, formats and g... view job details