Jobs at VERO Biotech

Leads hands-on manufacturing engineering, including equipment troubleshooting, automation, process improvement, equipment design and qualification, production data analysis, dashboard maintenance, and regulated documentation. Supports manufacturing scale-up, design transfers, validation, change controls, root cause analysis, and quality compliance. Provides technical leadership and mentorship while collaborating with Operations, Quality, R&D, IT, suppliers, and production teams.

Develop and validate dosing algorithms and component models for an inhaled nitric oxide delivery platform. Build simulations, test tools, and data-driven experiments in Python, then translate validated algorithms into production C/C++ embedded firmware. Integrate sensors and electromechanical hardware, troubleshoot control and communication issues, document requirements and traceability, and support verification, regulatory submissions, and product launch. Progressively provide firmware technical leadership, design oversight, integration planning, and mentoring.

Supports daily HR operations, including benefits administration, employee records, I-9 and E-Verify processing, background checks, onboarding and offboarding, payroll and HR audits, performance review preparation, recruitment coordination, interview scheduling, HR communications, and confidential file maintenance.

Directs end-to-end supply chain operations, including purchasing, planning, warehousing, inventory control, supplier management, and product distribution. Develops strategies to improve margins, inventory turns, efficiency, and supply chain resilience. Leads ERP implementation, contract negotiations, regulatory compliance, continuous improvement, budgeting, and product-launch material planning. Manages and coaches supply chain teams while ensuring adherence to FDA regulations, cGMP, quality, and safety standards.

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.

Support administration of the Quality Management System including investigations (NCRs, CAPAs, deviations), training, change control, internal audits, documentation control, KPI trending, and regulatory compliance (FDA/ISO). Assist Director of Quality Compliance in root cause analysis, corrective/preventive actions, SOPs, and continuous improvement to maintain GMP compliance.