Teams at Vertex Pharmaceuticals

Lead QA oversight for analytical development and validation across cell & gene therapy programs. Ensure cGMP and global regulatory compliance, support method transfer, stability and reference standard programs, drive investigations and corrective actions, review/approve documentation and contribute to quality system standards and regulatory submissions.

Lead FP&A for the U.S. Kidney business, driving budgeting, forecasting, performance management, scenario planning, KPI definition, and cross-functional financial decision support to enable pre- and post-launch commercialization.

Lead GxP documentation and electronic lab systems support at the manufacturing center, overseeing SOPs/WIs/batch records, eQMS deviation/CAPA/change control, LIMS/MES/Tulip/electronic training, data reviews, KPI monitoring, process improvements, and management of a team.