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 (UPLC), and Size-Exclusion Chromatography with Multi-Angular Light Scattering (SEC-MALS)• 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• Supervised/Trained Reagent Manufacturing Associates I-II with daily SOPs and GDP

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 Particle Counter (LPC) and Ultraviolet detector (UV).• 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• Purchase of laboratory consumables and equipment• Training junior analysts in laboratory duties• Coordinate with team members to ensure all testing for finished products and stability samples is completed in timely manner

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), Differential Scanning Calorimetry (DSC), polarimeter, colorimeter, and conductivity• 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• Assisted in training analysts on methods/instrumentation• Used LIMS to report data for products

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