As a Senior Validation Engineer at Lubrizol Life Science, I develop and execute validation plans for aseptic formulation, fill lines, and finishing processes, packaging, labeling ensuring compliance with cGMPs, SOPs, and regulatory requirements. I evaluate and optimize various process equipment, including compounding, filling, packaging, labeling, and inspection systems, using design of experiments and sampling plans. I also oversee process development from equipment installation to documentation, resolving production issues and implementing fixes. With a strong background in commissioning, qualification, and validation, I have extensive experience in working with SCADA, PLC, HMIs, and MES, managing control system interfaces and audit trials. I have also contributed to the validation of fill/finish equipment, Serialization, sterilization critical utilities, and building automation systems in previous roles at Pfizer and Hetero Pharma, leading teams and participating in advanced monitoring studies. I have a comprehensive knowledge of aseptic processing, lyophilization, and lean manufacturing, and have authored multiple validation master plans, temperature mapping, and IQ/OQ/PQ protocols. 2