Singapore, Singapore
As a graduate of Nanyang Technological University with a Degree in Chemical and Biomolecular Engineering, my internship at MSD honed my abilities in digital transformation, quality standards improvement, process streamlining and . Our teams effort of site-wide transition from paper-based logbooks to digital platforms significantly enhanced operational efficiency. Leveraging my academic knowledge, I've successfully conducted gap assessments to ensure our site alignment with the global standards and contributed to the development of a simplified electronic log system. This initiative was designed to foster a culture of 'Right First Time' in logbook entries, underscoring my commitment to continuous improvement and digital innovation in manufacturing processes. I was also involved in streamlining multiple sitewide procedures through periodic reviews, conducting production analysis for Keytruda and have assisted in AVIM reject vial analysis project to identify the sources of error. I've also prepared, analyzed trends and hosted biweekly meetings regarding potential microbial growth.
• Significantly helped to drive the site-wide effort to transition all high complexity paper-based logbooks to new digital platform (i.e elogs) by independently creating electronic drafts with involvement of cross-functional teams and senior engineer as mentor. Conceptualized simplified version to encourage Right First Time in elogs. • Performed Gap Assessment for 3 different topics by understanding and identifying the gap between site practices and global requirements for Quality Standard Improvement Plan (QSIP). • Performed Gap Closure and streamlining of up to 10 local document and procedures to meet global requirements. • Prepared, analyzed trend and hosted biweekly site Micro tier of stakeholders using PiCore Process book. • Assisted with Merck Production System projects to build process optimization. • Prepared and analyzed Keytruda production data and trend using Manufacturing Execution System (MES) to be presented to site management team. • Assisted in Automatic Vial Visual Inspection Machine (AVIM) reject vial analysis project by identifying the source and types of error. • Supported day-to-day operations for Keytruda and Remicade manufacturing, including document change controls, periodic review of SOP, CAPA, deviation investigation and implementation of ad-hoc improvement and digital initiatives led together with area leadership
• Mapped out Skills Future Framework to Oiltanking On-The-Job/Task Evaluation • Built a Technical Skills Competency Database • Data Validation and Consolidation • Conducted a Manpower Hours Study for 4 Terminals in Singapore by coordinating with all the Operations Manager & Shift Leader • Designed the template and formula for the Manpower Study for future reference
• Coordinated the Safety Day event of the company • Designed the framework for the Digitalized Management of Product Introduction (MOPI), which involved multiple department heads. • Conducted a Key Performance Indicator Analysis for HSSEQ Department, which was presented at the management level • Participated in various safety risk and quality assessment such as Hazard and Operability study (HAZOP), Hazard Identification, etc. • Assisted in Root Cause Analysis for Incident Investigation using Bowtie-XP software. • Assisted in documentation works, day to day tasks and ad-hoc work • Coordinated the Safety Induction Course Video Shoot • Participated in multiple Gemba for ongoing site projects