Teams at VERO Biotech

Ensure supplier products meet prescribed quality and regulatory standards through audits, documentation review, inspections, testing, KPI monitoring, investigations, training, and supporting regulatory inspections and continuous improvement in a cGMP environment.

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.

Lead end-to-end R&D new product development programs for medical devices/combination products, coordinating cross-functional teams (R&D, Regulatory, Clinical, Quality, Manufacturing, Commercial) to meet FDA submission and commercialization milestones. Manage integrated schedules, risk identification/mitigation, validation and design control alignment, FDA interactions, executive communication, and resource tracking to ensure on-time delivery and regulatory compliance.