Conduct advanced data analytics to identify bottlenecks, reduce errors, accelerate batch release, and improve manufacturing reliability. Gather and document business requirements, create process flows, and support solution implementation. Design and validate GxP-, GMP-, GCP-, and FDA 21 CFR Part 11-compliant systems, including AWS-based digital platforms for Cell and Gene Therapy manufacturing. Develop APIs, microservices, automation solutions, and secure digital prototypes supporting regulated operations and real-time data visibility.