Jobs at VERO Biotech

Support development of a nitric oxide delivery device by building and modifying prototypes, executing engineering test protocols, collecting and analyzing data (Python/MATLAB/Excel), documenting design controls (ISO 13485), and assisting process development and pilot line activities in a regulated medical device environment.

Lead post-market surveillance for combination products across two sites, owning complaint intake, triage, investigation, regulatory reporting, and closure. Ensure compliance with FDA regulations and international standards, oversee MDRs and corrections, integrate pharmacovigilance and device vigilance, drive risk-based investigations and CAPA alignment, and maintain inspection-ready complaint handling processes.

Lead and execute software and firmware development for a medical device platform, owning architecture, requirements, verification, release, and sustaining. Act as a hands-on manager: code and design reviews, defect triage, roadmap delivery, cross-functional collaboration with clinical, hardware, quality/regulatory, manufacturing, and service to ensure regulatory-compliant, high-quality product releases.

Territory-based account executive responsible for growing hospital utilization of Genosyl inhaled nitric oxide systems. Qualifies accounts, negotiates contracts, provides training, executes launches, manages CRM, develops strategic account plans, collaborates with clinical and respiratory specialists, and meets sales quotas.

Provide clinical training, education, and technical support for VERO Biotech respiratory products to customers and internal staff. Plan and run clinical evaluations, maintain documentation and vendor credentials, support clinical research and case reviews, represent the company at events, perform on-call duties, and travel frequently to service Northern California/Bay Area customers.