Erica Jane Eje

Experience

• 

  Duopharma Trade Phils., Inc

  Oct 2016 - Nov 2016

  Intern

  • Exposure on bioavailablity process and equipment• Implemented physical and digital filing systems for company documents• Daily checking of laboratory and office (GLP)

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  Integrated Manufacturing Services Providers Inc.

  Jan 2018 - May 2021

  Quality Assurance Analyst II

  • Completed daily reports of incidents, non-conformances, in-process, finished product and customer complaints product evaluation reports • Assess change control documents, risk management reports and risk analysis evaluations o Established Microbiology Laboratory – from acquiring materials, procedures, work instructions to microbial testing and generation of database and analysis reports• Produced various procedures, policies and work instructions for process improvement of current Quality Management System and Halal Assurance System • Controls monitoring, update, registration, retention and archiving of all kinds of documents and records per department• Reviews and updates existing procedures and policies for Quality Department and has been able to provide assistance and process development to other department such as Supply Chain, Warehouse, Procurement, Technical Services (R&D) and Production • Provides technical background as a team member to Pharmaceutical Expansion Project of IMSPI• Conducts training and refresher courses to all employees concerned regarding cGMP, HAS/ Halal Awareness, Food Safety, HACCP and knowledgeable with PIC/S GMP • Generates Internal Audit Report, Corrective and Preventive Actions for various type of incidents – GMP or non-GMP related including internal audit and customer complaint findings • Delegated to attend external trainings regarding Food Safety, Good Laboratory Practices and cGMP • Implemented and ensures strict compliance of all departments to current Quality Management System• Exposed to business continuity and business improvement • Trained and knowledgeable on pest control system and controls 5S checking and monitoring• Experienced and knowledgeable to audits – 3rd party and/or regulatory audits Show less

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  SGS

  May 2021 - now

  • Able to perform, analyze, troubleshoot and highly experienced in software applications of several equipments such as Agilent, Perkin Elmer and Waters HPLC system and Agilent HPLC/MS• Conducts method validation and method verification• Analysis of samples using High Performance Liquid Chromatography Equipment (HPLC) (Examples: Vitamins A, C, D3, B Vitamins, Biotin and Preservatives)• Prepares necessary solutions and reagents needed for the analysis incorporating good laboratory practices in the process• Monitors stock reagents, standards and ensures the minimum stock level quantity is maintained• Coaches lab analysts I, lab technicians, lab aides and OJTs on the performance of test, analyses, and sample preparation• Complies with Quality, Health and Safety protocols being implemented • Maintains laboratory workplace safe and orderly condition. Ensures that all laboratory supplies are available and within the minimum stock level• Analyzes and interprets standard laboratory test results including statistical quality control charts and uncertainty of measurements• Maintains routine documentation, including worksheets, log sheet entries, sample documentation, etc. Records data precisely and accurately. Signs worksheet and job instructions• Reports all incidents, including near misses and hazards, that may affect the achievement of QHSEE objectives in accordance with SGS Incident Reporting and Management requirements• Knowledgeable and experienced with ISO and Integrated Management System – ISO 9001, ISO 14001, ISO 45001, ISO 27001, ISO 50001, FSSC 22000, ISO 22301, ISO 13485 Show less

  • EHS Data Validator (Canada)

    Aug 2023 - now

  • Laboratory Analyst I-II

    May 2021 - Aug 2023