Chris Chan Email & Phone Number

San Jose, CA, US

San Carlos, California, United States

• Performed analysis on POI products and stability samples using the following analytical instruments: High Performance Liquid Chromatography (HPLC), Colorimetric methods, and Ultra Performance Liquid Chromatography.
• Maintain Good Documentation Practices (GDP) and Good Manufacturing Practices (cGMP) with data documentation and integrity
• Assist with method development for POI products and stability study reports
• Investigate and troubleshoot analytical methods for POI products and customer’s issues
• Train lab assistants in laboratory methods
• Assist with relocation affairs to three different sites

Redwood City, California, United States

• Coordinated with manager/supervisor/teammates on manufacturing duties with commercial products
• Advised Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP) protocols with data documentation and integrity
• Followed/Performed Reagent Manufacturing Standard Operating Procedures (SOP)
• Authored/Collaborated with Quality Assurance with Nonconformance Event Reports (NER)
• Uploaded/Printed/and Navigated documents through MasterControl
• Authored/Executed validation protocols

Fremont, California

• Perform analysis on finished products and stability samples using the following analytical instruments: High Performance Liquid Chromatography (HPLC), Gas Chromatography-Flame Ion Detector (GC-FID), Dissolution, Liquid.
• Maintain current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP) with data documentation and integrity
• Revise analytical methods, test protocols, standard operating procedures (SOPs) and stability reports
• Investigate and author Out-of-Specification(OOS)/Out-of-Trend(OOT) investigations reports
• Responsible for coordinating stability program which includes: authoring reports, revising protocols, arranging storage, and scheduling of testing
• Maintain laboratory equipment which includes: scheduling of preventative maintenance, coordinate vendor calibrations, and execution of installation qualifications

Columbia, South Carolina

• Followed cUSP, cGMP and SOPs to analysis: active pharmaceutical ingredients (APIs), excipients stability, finished products in process samples using cGMP lab practice
• Performed analysis using: general wet chemistry, Thin Layered Chromatography (TLC), titrations (manual and with auto titrator), Karl Fischer (KF), GC, HPLC, UPLC, Infrared (IR), UV, Total Organic Carbon (TOC).
• Performed monthly/weekly utility tests per cEP, cUSP, and SOPS
• Calibrated analytical balances and various instrumentation weekly
• Performed light maintenance/repairs of instrumentation
• Qualified for various gowning stages

Rock Hill, SC

• Followed SOPs and ISO guidelines to analyze samples using: general wet chemistry techniques, titrations,
• HPLC, GC, Ion Chromatograph (IC), UV, TOC, KF, and conductivity
• Performed weekly/monthly safety and housekeeping inspections
• Performed maintenance and troubleshoot analytical instruments
• Supervised/Trained Quality Control Chemist I in laboratory duties
• Followed 5S organization guidelines

Rock Hill, SC

• Followed SOPs and ISO guidelines to analyze samples using: HPLC, GC, IC, UV, TOC, Karl Fischer, Cyclic Voltammetry Stripping Polarograph (CVS), Atomic Absorption Spectrometry (AAS)
• Performed wet chemistry techniques to analyze acid/alkaline products using: pH, titration, specific gravity, colorimetric, and conductivity
• Performed formulation for manufactured products
• Calibrated pipettes, pH meters, and analytical instruments for accurate results
• SAP knowledge

• Followed SOPs to prepare: reagents, eluent, solutions, standards, and samples for daily analysis
• Performed daily analysis using: appearance, pH, titrations, IC, GC, and HPLC
• Recorded daily analysis results in detailed log book