End-to-end developer for key AI products and features leveraging frontier AI models and techniques, deployed at scaleSubject matter expert and trail blazer for AI and ML initiatives, providing guidance on delivering real business value with maximum return on investmentAligned project concepts, requirements, and feasibility, with high-level company objectives and championed development needs and priorities to company leadershipResearched state-of-the-art models, techniques, and tools, and prototyped implementation, to examine viability for productization and deploymentBuilt data pipelines including data sourcing, exploration, cleaning, bootstrapping, and processingContributed to AI products in the security, healthcare, and NLP domainsManaged and collaborated with varied teams from a wide variety of experiences, backgrounds, and levels of technical expertiseStrategic leader and counsel for seed stage startups, acting with implicit approval of CEO

Advanced Statistics for Machine Learning, Agent Based Modelling, Amazon AWS Cloud Computing, Artificial Neural Networks, Continuous Optimization, Data Assimilation, SQL, Deep Learning with Python, Project Management & Agile Framework, Metaheuristics, SAS, Semantic Web, Statistical Analysis of Massive & High Dimensional Data, Survival Analysis, Hadoop & Spark Ecosystem, Time Series Analysis

Preparing regulatory submission material for nine products at various stages of development including marketed, Phases I, II, III and during major submissions (NDA, MAA, IND) while ensuring content and data integrity throughout. Delivering accurate, submission-ready materials which meet or exceed regulatory agency standards. Leading Document Processor for recent MAA and NDA submissions, overseeing global work assignments, document inventory tracking and submission scheduling. Team systems and technology subject matter expert including document management system, SharePoint, and citation database.

As a member of the Regulatory Operations team I ensure that all regulatory submission material from across the company adhere to Gilead as well as FDA and/or global standards and are ready on pace with our accelerated submission schedules. I've also spearheaded our team's systems and technology initiatives including intranet development, document management system updates and cross-functional systems alignment and streamlining.

-Identification of desired antibody-producing hybridoma cell by Western blot-Plan and schedule hybridoma supernatants for testing against appropriate controls-Load and run Western blot gels using proper sterile technique-Transfer completed gels to PVDF membranes-Develop membranes with appropriate washes, secondary antibodies, and darkroom transfer to film-Digitally log all relevant test data-Track incoming hybridoma fusions and prepare necessary controls, secondary antibodies and materials

-Operation of autoclave-Pouring agar plates using sterile technique-Preparation of buffers within given pH parameters-Cleaning lab glassware using sterile technique-Ordering and supplying all necessary chemicals and materials for lab groups-Maintaining and facilities and equipment-Unlocking and locking facility doors and equipment stores at beginning/end of day