---Stem Cell Therapy Process Engineer----Designed and led cross functional equipment evaluation experiments for network fleet concept-Learned, executed and taught stem cell therapy manufacturing processes-Executed developmental studies for process improvement for stem cell therapies-Started and implemented 5s program ---CDMO Site Manager----Negotiated, implemented and managed with external vendors for a phase II clinical study-Primary Business and Project Lead for internal business and CDMO collaborator-Leading cross functional teams through the selection of a CMO for development and manufacturing services for a regenerative medicine product.-Actively managed budgets and consultants ---Cell Therapy Manufacturing Engineer----Played a pivotal role in the start-up of HIT's Cell Therapy Program, providing on-the-floor support that led to successful training and shakedown runs.-Developed SOPs for cell therapy manufacturing equipment, ensuring adherence to regulatory standards.-Automated batch record calculations, reducing manual effort significantly during the Cell Therapy project's start-up phase.-Ordered additional equipment and materials, enhancing the efficiency of newly constructed Cell Therapy Suites.-Created a comprehensive Manufacturing training curriculum, resulting in an improvement in onboarding times for Manufacturing Specialists.---Process Engineer----Spearheaded installation and operational qualifications for the Vanrx Modular Filler System, ensuring its compliance for syringe production, resulting in a 15% increase in production efficiency.-Developed and implemented safety changes for VPHP Exhaust, contributing to reduction in safety incidents during the commissioning phase.-Led a team to optimize syringe stoppering positions, resulting in a reduction in stoppering errors.-Introduced a new measurement method for syringe insertion depth, streamlining the qualification process and saving 10% in time and resources.