Cheyenne Roth Email and Phone Number

- Supported the setup of a start-up laboratory that provides formulation development for precision delivery of probiotics and micronutrients for oral administration- Key member of the formulation team and microbiology team on the probiotic formulation development project- Evaluated material-probiotic interactions to understand how leading material choices for formulations affect probiotic viability- Developed and conducted experiments to evaluate encapsulated probiotic formulation performance regarding resistance against biological challenges and accelerated storage conditions in various food matrices- Produced 75+ encapsulated probiotic or carotenoid prototype formulations with varying payloads with a small team using bench scale methods such as spray chilling, extrusion and milling, pan coating, melt emulsions, etc. - Crafted and screened 150+ GRAS material blends for moisture barrier properties for formulation material selection- Traveled to partner CMOs to document manufacturing process and process parameters as well as communicating any necessary corrective actions during the manufacturing process of the desired probiotic formulations- Assessed encapsulated probiotic formulations produced at pilot scale CMOs- Supported microbiology team needs such as media preparation, plate pouring, plating and colony enumeration- Analyzed and presented experimental data to internal team of scientists and management- Authored formulation equipment SOPs and experimental protocols- Listed as an inventor on multiple pending patents

- Authored qualification relevant documents such as risk assessments, installation and operational qualification protocols, engineering studies, and protocol final reports- Executed equipment validation studies within a collaborative cross functional team environment- Performed data analysis throughout engineering studies for determination of acceptable results and project direction- Conducted validation deviation investigations to identify root causes and define corrective/preventative actions- Subject matter expert for validation department analytical instrument data logger system used to perform controlled temperature/humidity chamber qualifications- Supported the review and approval of non-validation scope documents needed to start production and qualification activities such as preventative maintenance forms, calibration forms, and SOPs

- Independently conducted viability assays in vitro to analyze antimicrobial properties of biopolymers- Cultured bacteria such as E. coli and S. aureus- Prepared media and reagents for all experiments- Utilized equipment such as micropipettes, autoclaves, centrifuges, spectrophotometers, and CO2 incubators- Applied wet chemistry techniques for concentration and pH testing- Created SOPs for any conducted experiments

- Assisted in Commissioning Qualification and Validation effort for Facilities, Utilities, Systems and Equipment for cGMP purposes- Assisted in the development, fabrication and equipment testing in support for development and manufacturing operations- Created and maintained documentation following cGMP and GLP proceduresfor specifications (SOP,URS, FS, etc.)- Project head for Commissioning Test Plan Audit- Assessed eTOPs for use of biotech equipment such as bioreactors, centrifuges, and chromatography- Generation and analysis of field and technical report

• Table top management• Reservation system management• Service layout customization• Staff training

• Product design and placement for events• Product packaging and distribution• Fulfillment of custom orders

• Guest and reservation management• Food delivery and preparation assistance• Customer care and accommodation