On market design change quality engineer. Ensure product safety and effectiveness by guiding sustaining and development teams on design controls, risk management, and compliance (ISO 13485, FDA), serve as a quality expert on project teams, facilitating root cause analysis, and driving quality system improvements for genomic tech products. As a senior-level quality representative maintain and demonstrate deep technical understanding, cross-functional leadership, and ensure quality throughout the product lifecycle, from concept to market, impacting health equity. Key responsibilities: Quality Oversight, QMS & Process Improvement, Design Control, Risk Management, Regulatory Compliance, Design History Files, and Audit support.

On-Market design quality engineer supporting changes to Illumina's consumable portfolio changes. Cross functional core team member on PMT, reviewing and triaging changes, quality investigations, customer complaints, and resulting activities and communication. ctively manage and participate in design control activities, including research and diagnostic applications. Ensure product and process conformance to applicable safety and quality system regulations and standards (e.g. FDA (820), ISO 13485, ISO 14971, IVDR). Guide project teams on execution of design control activities in alignment with quality system requirements and current best practices to ensure the company's products and processes are safe, effective, and meet customer performance needs. Representative for total quality on cross functional project teams. Key Responsibilities: Quality Oversight, Risk Management, Documentation, Audits, CAPA, and Design History File management.

Operations quality focused on field failures and returned material.

Working in the iDepot department to refurbish, upgrade, and troubleshoot Illumina HiSeq and MiSeq instruments. Primary job function is the management of daily activities for the floor operators, tracking instrument orders, prioritizing efforts and communicating with planning and management on status updates. Additional tasks include; participating in escalations from the field on instrument installations or problem instruments, approving deviations from manufacturing processes, approval of replacement parts, leading quality improvement projects, and optimizing manufacturing work instructions.

I managed intelligence collection teams operating in the NATO mission in Kosovo. Guided the teams targeted asset collection, provided quality control and publishing authority on reports generated by the teams, and oversaw their daily activities. I liaised with US Embassy staff to coordinate and share information and prevent overlapping assets. Worked with the intelligence leadership to develop intelligence requirements, that when answered, provided theater commanders the tools to develop courses of action which reflect the operating environment and aligned with the interests of the United States and our NATO partners.