Working as a Sterilization Specialist• Perform technical review of incoming work to determine test appropriateness and sample requirement.• Guide and discuss validation/routine testing programs for medical devices and pharmaceuticals with the clients and develop Client Testing Requirements (Test Specification) according to ISO or USP guidance. o ISO 11137, 11135, 11737 o USP <61>, <62>, <51>, <1227>, <71>, <85>, <151>, <161> o AAMI ST72• Coordinate testing schedule with laboratory staff.• Review and sign routine GMP report for technical accuracy and completeness.• Draft and revise controlled documents (SOPs, Reports, Protocols, Test Methods, Test Specification, Worksheets, Etc.)• Investigate out of specification, unexpected results, nonconformance and develop CAPA, using TrackWise system• LIMs, Master Control• MicroSEQ analysis

• Performed laboratory daily routine quality control and assurance tasks on cosmetic samples, raw materials, and bulk samples.o USP <61>, <62>, <51>,<1227>• Coordinated quality analysis to ensure accurate results, timely completion, and proper responses and notification.• Coordinated release of the QC products by efficiently and tactically communicating with document control and supply chain.• Performed environmental testing on air, surface, and water to ensure environments were controlled.

• Performed laboratory daily routine quality assurance tasks on beer samples such as pH, billings, alcohol, sodium, and iron. • Coordinated quality analyses ensuring accurate results, timely completion, and proper responses and notification. • Performed various studies and performed statistical analyses to improve quality throughout the brewery. • Performed routine testing of pasteurizers for proper pasteurization.

• Performed laboratory procedures and data analysis of DNA pertinent to the improvement of the existing HLA gene typing products and processes using Orchid, Fusion, and Microsoft Office programs.• Collaborated in SOP creation and revision to improve testing procedures, reflect the procedures' changes, and monitor the organization of all official documentation.• Trained new members of LABType on relevant procedures and machine hardware, arranged a training or meeting as necessary.• Designed and led the project as a project lead effectively and in a timely manner by prioritizing tasks and collaborating with others.o Managed meetings between R&D, sales, and production for product release schedule.o Managed meetings between the team and the management group to ensure the project was moving forward and required materials were ordered ahead of time.o Efficiently and tactically communicated with the team for the best result.o Created MS VBA programs to efficiently do data analysis.