Jobs at VERO Biotech

Leads strategic sourcing and contract manufacturing for new product development, sustaining engineering, and commercial operations. Responsibilities include supplier identification and qualification, RFQs, quote analysis, negotiations, contract manufacturer management, supplier performance, risk mitigation, cost reduction, dual sourcing, tooling and NRE planning, and spend tracking. The role collaborates with Engineering, Quality, Supplier Quality, and Operations to ensure supplier readiness, cost, quality, delivery, and production scalability.

Supports engineering projects for the GENOSYL DS medical device, including manufacturing and service process optimization, testing, data analysis, documentation, equipment and fixture validation, process improvement, and console repair or rework. Collaborates with engineering, R&D, and other teams to develop and validate manufacturing processes while presenting test results and creating SOPs and work instructions.

Supports project planning, scheduling, reporting, documentation, risk and issue tracking, stakeholder coordination, and PMO processes for a regulated nitric oxide delivery device development program. Maintains project plans, dashboards, action logs, and status reports while assisting with meetings, process improvements, design control documentation, and cross-functional communication.

Supports development of a nitric oxide delivery device, including prototypes, fixtures, consoles, and drug product cassettes. Executes engineering tests, operates laboratory equipment, collects and analyzes data, troubleshoots setups, and prepares reports. Assists with design improvements, manufacturing process validation, pilot line activities, and ISO 13485 design-control documentation in a regulated medical device environment.

Develops customized account-based marketing campaigns and sales enablement materials for strategic accounts. Partners with sales and leadership to translate customer, technical, clinical, and market information into persuasive visual stories, presentations, proposals, case studies, and digital content. Manages projects from concept through delivery, coordinates reviews, maintains brand quality and version control, meets tight deadlines, and tracks business impact. This is a full-time, on-site role requiring strong design, writing, editing, storytelling, and project-management skills.

Develop and maintain a C#/.NET medical-device application, improve architecture, testing, code quality, and documentation, and integrate software with GUI, firmware, operating systems, and hardware. The role clarifies requirements, supports regulated design controls and traceability, conducts code reviews, mentors developers, coordinates distributed and vendor teams, and contributes to Agile planning and technical leadership. This is an onsite position in Atlanta, Georgia.

Leads mechanical design and development of electromechanical medical devices from prototype refinement through design verification, manufacturing transfer, and production launch. Creates SolidWorks models, drawings, bills of materials, and technical documentation; integrates fluidic and electromechanical components; executes testing; investigates root causes; and improves designs for manufacturability, reliability, cost, and serviceability. Collaborates across engineering, quality, manufacturing, suppliers, and external teams while supporting design reviews, risk assessments, FMEAs, and technical leadership.

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.