EBR Systems, Inc. is a medical device company specializing in innovative cardiac rhythm management solutions, including the WiSE Cardiac Resynchronization Therapy system. The company develops leadless left ventricular CRT devices and provides comprehensive clinical support, training, and technical guidance to improve patient outcomes.
Open Positions
Manager/Sr. Manager, Product Support Engineering - Onsite (60% - 80% in office)
BS or MS in Mechanical Engineering or related field, 8+ years in Product Support Engineering, and ability to establish scalable engineering processes
Part-Time Sr. Payroll Specialist (Up to 20 Hours A Week)
5+ years of experience, Associate degree or bachelor’s degree in Accounting, Finance, or related field, and prior experience using Paylocity
Field Clinical Specialist - Southeast U.S.
11 years of relevant clinical support experience; or Associate degree plus 9 years; or Bachelor’s degree plus 7 years; or Advanced degree plus 5 years
CNC Machinist, Machine Shop Manager
12+ years of experience in CNC machining, AA or equivalent in machine technology, proficient with Mastercam, Surfcam, or equivalent software
Field Clinical Specialist - Northeast U.S.
High school diploma plus 11 years of relevant clinical support experience; or Associate degree plus 9 years of relevant clinical support experience; or Bachelor’s degree plus 7 years of relevant clinical support experience; or Advanced degree plus 5 years of relevant clinical support experience
Supply Chain Engineer
BS or equivalent, 5+ years in medical devices, NetSuite experience preferred
Senior Lead Quality Analyst - Post Market Surveillance
Bachelor's degree in a scientific discipline. 5+ yrs in Post Market Surveillance & complaint handling. Experience with AIMDs & FDA regulations is essential
Senior Quality Engineer (Electrical & Software Engineering)
BS in engineering field with software experience. 7+ years of experience. Strong understanding of regulatory standards for medical device industry, including IEC 60601. Proficiency in PE and software engineering
Principal Regulatory Affairs Specialist
Bachelor's degree in a scientific, engineering, or technical discipline, 7+ years of Regulatory Affairs experience, experience with Class III active implantable medical devices
US Director of Training
10+ years in the medical device industry, 5+ years of leadership experience, and expertise in FDA compliance, QMS integration, and global regulatory standards
+13 More Jobs Available!
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