MARIA RUOCCO

Accomplished biotechnology professional with extensive experience in gene therapy, viral vector production, and analytical development within GMP-regulated environments. Currently serving as a Manufacturing Supervisor at Lonza, leading production planning and overseeing operations in gene therapy manufacturing.

Progressed through scientific roles at Lonza from PD Scientist I to PD Scientist II, contributing to analytical method development, tech transfer, and GMP assay qualification. Experienced in developing SOPs, leading assay validations, conducting gap assessments, and training QC analysts across cell therapy and viral vector programs.

Brings a strong research foundation from Rice University and UC Santa Barbara, with additional experience in laboratory operations and teaching. Combines technical expertise with leadership and project management skills to drive efficiency, compliance, and innovation in biopharmaceutical development and manufacturing.v