Teams 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.