• Transferred classroom characteristics gathered from in person/online database assessments into online application.
• Booked academic room requests into Registrar-managed classrooms
• Supported timetabling and final exam schedule creation via online coding verification to ensure accuracy of schedule.
• Replaced and updated classroom emergency safety posters and room layouts from plant operations. Logged and tracked
these characteristics into online application.

• Reviewed 20+ Executed Batch Product records for compliance with company SOPs, updated and reviewed Deviation
Standard Operating Procedures (SOP) and Process Batch records.
• Assisted with trending reports, tracking performance for Quality Assurance (QA) team for Global Quality Council meetings.
• Updated and reviewed Consolidated Tables for Domestic Health Canada Drug Establishment Licenses (DEL) to assure
adherence with Health Canada guidelines.
• Prepared and organized documentation for company audit to ensure adherence to industry regulations and standards.
Participated in audit meetings and improved audit preparation processes and procedures with suggestions for better
documentation presentation.
• Liaised with manufacturing sites to request quality documents, review materials and coordinating batch corrections.
• Supported quality improvement projects, collected, and analyzed temperature excursion data from UPS Warehouses to
monitor storage conditions of various products. Advocated for process improvements to minimize product losses in the
warehouse by addressing unnecessary excursions that triggered quality department reviews.
• Archived Documentation as per retention policies

• Monitored, tracked and troubleshooted manufacturing processes related to process efficiency, product quality,
throughput, & yield at pharmaceutical CDMO (Contract Drug Manufacturing Organization)
• Assisted process investigations through data compilation and statistical analysis to determine root cause to atypical events
by identifying trends and presenting data to Senior Engineers such as Tablet Metal Rejects project.
• Created KPI presentations, presented analysis results, prepared trend and risk analysis reports (Annual Product Reviews).
• Contributed to process improvement projects as well as preparing and data checking technical reports by collecting and
analyzing data from Process Batch records, Lab Report Books, Formulation records and Bills of Materials.
• Took initiative in change management activities such as initiating change controls using Global Quality Trackwise and
SAP enterprise software to source information and navigate business operations.
• On floor liaison with Manufacturing Team for Process Engineering Support for Processing, Granulation, Compression,
Dispensing, Packaging, Production, Quality and site Engineering team.
• Completed process executions such as hand changes, revising Manufacturing Batch Records through Trackwise, liaising
with onsite visiting clients, implementation of new technology in processing and overseeing process improvement projects.

• Acted as lead for ensuring documentation readiness for LIMS related documentation/data by investigating onsite Logbooks.
• Created project plan with defined milestones and timelines to complete “Review of QA/QC Logbooks Project.”
• 0 overdue Compliance Wire SOP, EHS trainings, ensured compliance of cGMP, GDP and SOPs
• Reviewed 1500+ Logbooks for condition, issue date, active/inactive status. Revised and updated company documentation for
comments/recommendations for next phase of project.
• Archived 40+ Iron Mountain boxes of inactive Logbooks