Lola De Ubeda

I've led complex deviation investigations, CAPA programs, and quality improvement initiatives across pharmaceutical manufacturing sites for VIRBAC, Novo Nordisk, Curium, Laboratoires de la Mer, and Siemens Healthineers.

At VIQI for Novo Nordisk, I investigated environmental contamination and process deviations in classified areas using 5 Whys, Fishbone/5M, and Six Sigma. I designed and monitored CAPAs, built shopfloor visual-management tools and a digital deviation-traceability application, and coached operators on contamination risks, cleanroom behaviors, and cGMP compliance.

I've also delivered Change Controls for filling lines, cleanrooms, formulation, sterilization units, and R&D laboratory revamping projects. I coordinate Production, QA, EHS, Maintenance, IT, Facilities, and engineering contractors to evaluate quality, process, safety, and ergonomic impacts.

I use Power BI, Python, and VBA to automate KPI reporting and support practical, sustainable continuous improvement. My work is grounded in cGMP/EU-GMP, ISO 14644, ISO 9001, ISO 13485, data integrity, and inspection readiness.