Experience

PBF Energy

• United States
• Oil and Gas
• 700 & Above Employee

• Laboratory Technician

  • Feb 2020 - Present



Shell

• United Kingdom
• Oil and Gas
• 700 & Above Employee

• Lab Tech

  • Aug 2015 - Feb 2020

  Testing crude oil and petro products Testing crude oil and petro products



Impax Laboratories

• Pharmaceutical Manufacturing
• 200 - 300 Employee

• QC Chemist II

  • Nov 2014 - Jul 2015

  • Perform analysis of stability samples and finished products with HPLC, GC, UV, and dissolution tester to ensure products meet specifications• Report OOS, OOT or other laboratory result anomalies and investigate causes and propose appropriate corrective/preventative actions• Record data in controlled notebooks, data sheets and validated spreadsheets• Perform proper hazardous waste removal• Support in-process testing for production release and materials qualifications

• R&D Chemist III

  • Feb 2014 - Oct 2014

  • Perform analysis of raw material, in-process and finished products with HPLC,GC, UV, and FTIR by following SOP• Develop and validate testing methodology, including drafting protocols, analyzing data results/trends and report writing• Report OOS, OOT or other laboratory result anomalies and investigate causes and propose appropriate corrective/preventative actions• Compile and analyze laboratory data for quality and technical trending, and for specification recommendations• Maintains proper documentation and lab practices in accordance with cGMP and company SOPs• Perform peer review of other staff results and documentation• Provide technical, quality, regulatory guidance to lower level staff



Dow Pharmaceutical Sciences

• Petaluma

• R&D Chemist II

  • Jan 2008 - Feb 2014

  • Analyze topical products and stability samples with Agilent HPLC following Testing methods and SOPs • Develop HPLC methods under team leader’s supervision • Validate HPLC methods and assist in preparing reports • Perform Out Of Specification, deviations and other technical investigations • Complete projects in a timely manner • Perform peer review of other staff results and documentation • Analyze topical products and stability samples with Agilent HPLC following Testing methods and SOPs • Develop HPLC methods under team leader’s supervision • Validate HPLC methods and assist in preparing reports • Perform Out Of Specification, deviations and other technical investigations • Complete projects in a timely manner • Perform peer review of other staff results and documentation



Stason Pharmaceuticals, Inc.

• Irvine

• Chemist

  • Jun 2003 - Jan 2008

  • Analyze solid dosage products and raw material with Waters HPLC, Agilent GC, UV-VIS, and dissolution tester following Testing methods and SOPs • Train junior chemists and lab technicians in various methodologies • Maintain various instrumentations in the QC laboratory to ensure compliance with cGMP • Prepare, review and revise Standard Operating Procedures for QC laboratory • Validate analytical methods and prepare report • Perform Out Of Specification, deviation investigations • Assist in FDA audit responding to all QC inquiries • Perform peer review of other staff results and documentation



Standard Chem & Pharmaceuticals, Inc.

• Taiwan

• QC CHEMIST

  • Oct 2001 - Feb 2003

  • Analyze solid dosage products and stability samples with HPLC, GC, UV-VIS and dissolution tester • Train junior chemists in various methodologies • Review and revise Standard Operation Procedures for QC laboratory • Perform peer review of other staff results and documentation • Assist in Bureau of Medical Affair (FDA equivalent in Taiwan) audit • Validate analytical methods and prepare report • Perform Out Of Specification, deviation investigations • Analyze solid dosage products and stability samples with HPLC, GC, UV-VIS and dissolution tester • Train junior chemists in various methodologies • Review and revise Standard Operation Procedures for QC laboratory • Perform peer review of other staff results and documentation • Assist in Bureau of Medical Affair (FDA equivalent in Taiwan) audit • Validate analytical methods and prepare report • Perform Out Of Specification, deviation investigations



Tera Pharmaceutical, Inc.

• Buena Park, CA

• QC Chemist

  • Dec 2000 - Jun 2001

  • Analyze injectables and stability samples with GC, HPLC • Maintain HPLC, GC and various laboratory instrumentations • Analyze raw materials using wet chemistry techniques • Document all pertinent laboratory duties according to Standard Operation Procedures • Analyze injectables and stability samples with GC, HPLC • Maintain HPLC, GC and various laboratory instrumentations • Analyze raw materials using wet chemistry techniques • Document all pertinent laboratory duties according to Standard Operation Procedures



Truesdail Laboratories, Inc.

• Tustin CA

• Chemist

  • Aug 2000 - Nov 2000

  • Analyze municipal water and industrial waste water samples utilizing EPA methods • Maintain GC • Prepare report for testing results • Analyze municipal water and industrial waste water samples utilizing EPA methods • Maintain GC • Prepare report for testing results