Vera Silva

Background

About Vera Silva

With over 10 years of experience across industrial production, R&D, and quality-driven medical device development, I bring a solid foundation in GMP-compliant manufacturing, process validation, and data-based process optimization. Skilled in RStudio for data analysis and visualization, I leverage data insights to improve product quality, streamline operations, and support regulatory submissions (CE and FDA). My hands-on experience includes bioreactor operation, wastewater treatment, and the integration of environmental and process engineering principles to ensure sustainability and compliance. I’m passionate about turning complex technical data into actionable strategies that enhance quality, efficiency, and regulatory readiness. Driven by precision, collaboration, and continuous improvement, I aim to contribute to high-performing pharmaceutical and biotech environments.