Experience

Perrigo AU

• Pharmaceutical Manufacturing
• 1 - 100 Employee

• QC Chemist

  • Jul 2017 - Present

  • Maintains product quality by chemical analysis as per current test methods and Standard Operating Procedures (SOP’s). • Ensures the quality of Intermediate bulks and Finished Pharmaceutical products of the company through different instrumental and wet chemistry analysis such as GC/FID, UPLC and HPLC Empower, Karl Fisher titration, FTIR, UV/VIS as per established analytical procedures. • Investigates deviations and writes Testing Deviation and Investigation Report (TDI) to ensure the company provides excellent product quality to end consumers. Empowers GMP and company requirements by documenting experimental results and ensures top performance of testing equipment by calibration and basic maintenance within agreed timelines. Show less



Pfizer

• United States
• Pharmaceutical Manufacturing
• 700 & Above Employee

• QC Chemist

  • Jun 2015 - Jul 2017

  • Maintains product quality by carrying out routine and experimental work as per current test methods and Standard Operating Procedures (SOP’s). Investigates deviations and writes VDF/LIR/QAR/CDN as to ensure the company provides excellent product quality to end consumers. • Empowers GLP and company requirements by documenting experimental results, checking results of other analysts to ensure complete accuracy of data. • Ensure top performance of experimental equipment by commission and validation of new laboratory instruments and preparation of validation documentation within agreed timelines. Show less



Imtrade CropScience

• Australia
• Chemical Manufacturing
• 1 - 100 Employee

• Chemical Technician Officer

  • Jul 2010 - May 2015

  • Ensures excellent product quality by sampling of incoming formulated and fully formulated agrochemical products and performs QC routine testing via physical laboratory tests and instrumental analysis (HPLC,GCFID and FTIR); • Reviews and evaluates inspection findings, test results and batch documents; • Recommends release/rejection of incoming formulated and fully formulated agrochemical products; • Performs HPLC and GC/FID method validation in compliance of GLP and provide reliability of test method used for analysis; • Supports business operation by providing good quality products during packaging processes based on the requirement of the work order; • Maintains product quality during formulation by applying good manufacturing processes and maintains safety at the workplace. Show less



Unilab, Inc.

• Pharmaceutical Manufacturing
• 700 & Above Employee

• Quality Assurance Inspector

  • Feb 2009 - Jun 2010

  • Conducts routine inspection and sampling of incoming raw materials;• Reviews and evaluates inspection findings, test results and batch documents;• Recommends release/rejection of raw materials for production use;• Prepares deviation reports and recommends solution/actions via SAP Quality Notification;• Conducts investigation and troubleshooting activities on problems encountered in production and warehouse;• Promotes teamwork by training lower level inspectors and laboratory aide;• Conducts retrospective data analysis to generate quality and/or productivity improvements and works on special projects for quality and/or productivity improvements. Show less

• SAP Quality Management Master Data Administrator

  • Apr 2007 - Jun 2010

  • Represents the SAP Project Phase 2 Quality Management in improving the QA business process;• Regularly worked on system improvements to increase productivity and generate materials and man-hour savings of the work unit/ department.• Develops the SAP Quality Management Master data for improving the business process of the Quality Assurance Division ;• Conducts user acceptance and end user training to business owners for easy navigation and execution of SAP QM module;• Evaluates existing QA business process and integrating it with either using the standard or customizing the SAP Quality Management module Show less

• Laboratory Analyst

  • Oct 2002 - Apr 2007

  • Ensures the quality of raw materials and finished pharmaceutical products of the company by using the Shimadzu High Performance Liquid Chromatography Class VP and Class GC system;• Performed chemical analysis via preparation standard and sample assay based on documented laboratory procedures;• Recommends acceptance or rejection of incoming raw materials of finished pharmaceutical products based on laboratory results versus set specifications;• Issues Exception Report on deviations observed concerning the quality results;• Ensures proper documentation of all information pertinent to the Quality Analysis;• Assures the suitability of the chemical testing procedures by performing Analytical Methods validation;• Promotes teamwork by training newly hired laboratory technicians on chemical assay preparation and basic HPLC instrument operation. Show less

• Laboratory Technician

  • Jun 2002 - Oct 2002

  • Ensures the quality of Finished Pharmaceutical products of the company via Dissolution Testing;• Performed chemical analysis by preparing standard and sample assay based on documented laboratory procedures;• Ensures proper documentation of all information pertinent to the Quality Analysis;• Ensures that Current Good Laboratory Practice (cGLP) requirements are adhered to throughout the validation exercise.