Jacqueline Tio Email & Phone Number

San Francisco, CA, US

Hayward, California, US

South San Francisco, California, US

-Good Manufacturing Practices (GMP) -Biologics/Vaccine R&D QC-Responsible for conducting analysis of raw materials, in-process samples, Active Pharmaceutical Ingredients, and other requested testing according to Standard Operating Procedures, GMP, and other regulatory requirements-Maintained laboratory equipment and Calibration; including troubleshooting.

San Francisco, CA, US

-QC R&D and GMP specialist for small molecule and biologics products.-Performed Analytical Testing for various drug substances, drug products and other materials according to approval methodology.-Trained New Hires-Authored, Revised, and reviewed SOPs, qualifications, validation protocols, and reports.-Owned and Executed Deviation reports, Change controls.

South San Francisco, California, US

• Designed and prepared formulations for small molecules in discovery and development.
• Conducted experiments to determine the physical and chemical properties of small molecules in discovery and early stages of development.
• Oral dosage formulation development and physical characterization activities.
• Analytical-related activities including method development, operation, qualification of HPLC anddissolution testing apparatus.
• Met with Research groups for project meetings and prepared data for presentation.
• Drug Product development activities from the research stage through cGMP manufacture in a phase- appropriate manner for various dosage forms for oral tablets.

Foster City, CA, US

• Prepared and analyzed pre-clinical formulation stability studies.
• Performed Characterization and stability tests on formulations and components including HPLC/UPLC,solubilities, and various analytical assays.
• Managed project timelines and schedules to ensure deliverables were met and the product is shipped accurately to CRO for testing.
• Performed data analysis and ensured documentation is recorded accurately and complied with GDPguidelines and company policies.

Wayzata, Minnesota, US

• Quality Testing for Low Calorie Sweetener (HPLC, JECFA assay, HPLC, GC, TOC,ICP, Heavy Metals)
• Bioassays: Yeast & Mold
• Instrument Calibration and Maintenance (HPLC, GC, TOC)
• Regulatory Compliance Audits: executed routine audits in compliance to ISO and GMP regulations.
• Managed laboratory inventory and procurement of reagents, raw materials, and other laboratory supplies.
• Partnered with the R&D team to validate methods and instrumentations.

Wayzata, Minnesota, US

• Managed Quality Control Processes: Oversaw the quality control procedures for the release of raw materials and final products, ensuring adherence to quality standards.
• Conducted Analytical Testing: UV-Vis, visual inspection, moisture, aflatoxin testing and production line check.
• Resolved Quality Related-Issues: Investigated and addressed internal and external quality issues by conducting comprehensive root cause analysis and implementing timely CAPA.
• Handled Out-of-Specification Results and Special Projects

Wayzata, Minnesota, US

Managed Quality Control Processes: Oversaw the quality control procedures for the release of raw materials and final products, ensuring adherence to quality standards.Conducted Analytical Testing: UV-Vis, visual inspection, moisture, aflatoxin testing and production line check.Resolved Quality Related-Issues: Investigated and addressed internal and.

Master'S Degree, Health Policy And Law

High School, High School Diploma

Bachelor’S Degree, Biochemistry Minor In Political Science