Apply knowledge of Proteomics to adapt or design computer systems. Responsible for working on biological manufacturing processes for formulation of COVID-19 vaccine including but not limited to Analytical, Upstream, Downstream and Fill Finish manufacturing equipment's. Review records and perform real-time review during validation of manufacturing operations and supporting documentation for completeness, accuracy and compliance. Performing gap analysis, requirements gathering for projects with the vendor and cross functional teams. Review and address the deviations associated to different issues across the platform. Perform audits of manufacturing and support areas, including in-process batch record review for adherence to internal procedures and industry best practices. Track and trend data on a weekly basis to update the project timeline and daily work. Detect coaching needs and take actions in accordance with these needs to ensure compliance with quality standards. Elaborate the procedures of sampling and guidelines for collection and reporting quality data. Oversee the implementation and ensure efficiency of inspection and quality systems. All of the above duties will be performed using a wide variety of tools mainly using Validation, & Analytical/Mathematical Skills.