Experience

Floré by Sun Genomics

• United States
• Biotechnology Research
• 1 - 100 Employee

• Sanitation Officer

  • Apr 2023 - Present

  San Diego, California, United States

• Quality Engineer

  • Dec 2022 - Present

  San Diego, California, United States Responsible for quality department daily operation and compliance of ingredients & final product with UL and company standards, as well as supporting GMP manufacturing, and supply chain & logistics for a small biotech startup company. Responsible for materials testing in cGMP manufacturing & recurring contamination screening, quality and sanitation final signoffs, process development of products, projects, and procedures for food supplement probiotics. Regularly involved in process… Show more Responsible for quality department daily operation and compliance of ingredients & final product with UL and company standards, as well as supporting GMP manufacturing, and supply chain & logistics for a small biotech startup company. Responsible for materials testing in cGMP manufacturing & recurring contamination screening, quality and sanitation final signoffs, process development of products, projects, and procedures for food supplement probiotics. Regularly involved in process optimisation, troubleshooting and scaling of manufacturing practices in a growing startup environment using GMP.

• Quality Engineering Intern

  • Aug 2022 - Dec 2022

  San Diego, California, United States



University of California San Diego

• Volunteer Ph.D. research assistant

  • Aug 2022 - Oct 2022

  San Diego County, California, United States Assist in the creation of laser cut, copper shadow masks for the fabrication of field effect transistors being developed and researched by graduate and Ph.D. students at UC San Diego



Floré by Sun Genomics

• United States
• Biotechnology Research
• 1 - 100 Employee

• Process Engineering Intern

  • Apr 2022 - Jun 2022

  San Diego, California, United States Assist Sr. process engineer to compile & create documentation and procedures required to meet ANSI & FDA standards for dietary supplements in anticipation of UL audit and certification of the manufacturing process. Review, update, and create: SOP’s, safety & emergency protocols, quality assurance & testing procedures, cataloging & sample tracking forms, research and assure compliance with audit and FDA guidelines for a custom manufacturing process.