BiVACOR, Inc.
Field Clinical Engineer
United States · Staff+
Sponsorship not specified$130k-$180kDetected 48 days ago
Electrical EngineeringFDA RegulatoryMedical DevicesCommunication
About the role
- As a Field Clinical Engineer at BiVACOR, you will be the on-site technical authority, partnering with surgical teams, ICU staff, and hospital biomedical engineers to ensure safe, effective device operation from implant through long-term follow-up.
- You will bring sharp technical instincts, composure under pressure, and a commitment to excellence that helps move us closer to transforming care for patients with end-stage heart failure.
- Train surgical teams, ICU staff, and hospital biomedical engineers on device operation and troubleshooting
Responsibilities
- Conduct pre-implant readiness checks, intraoperative support, and post-implant follow-up at assigned sites
- Document device performance, incident reports, and site interactions in the clinical database
- Contribute to the development and refinement of field support SOPs and training materials
Nice to have
- Bachelor's degree in Biomedical Engineering, Electrical Engineering, or a related field
- advanced degree preferred
- Prior experience with cardiac assist devices, ECMO, VAD, or implantable systems strongly preferred
Skills
- Can-do attitude - composure under pressure - strong teamwork and communication skills
Compensation
- The expected salary range for this position is $130,000 to $180,000.
Benefits
- BiVACOR offers a competitive compensation package and comprehensive benefits, including:
- Medical, dental, and vision insurance
- Health Savings Account (HSA) & Flexible Spending Account (FSA)
- Life insurance & Employee Assistance Program
- Generous paid time off
- A discretionary annual bonus may be available based on individual and Company performance.
- This position also qualifies for the benefits detailed at the link provided below.
- Relocation benefits are not available for this posting.
- 3-5+ years of field clinical engineering or field service experience in a Class II or Class III medical device environment
- Strong understanding of FDA QSR (21 CFR 820), ISO 13485, and medical device complaint handling requirements
Company info
- 401(k) with company matching
- Apply today and be part of something extraordinary.
Equal opportunity
- equal opportunity employer.
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