I bring over three years of experience in pharmaceutical manufacturing, regulatory affairs, and health informatics. Currently enrolled in the Graduate Certificate in Pharmaceutical Regulatory Affairs and Quality Operations at Seneca Polytechnic, I am focused on enhancing my skills in regulatory submissions, quality control, and continuous improvement. My technical expertise spans Lean Six Sigma principles, data analysis, and visualization tools like Power BI, Excel, and Tableau, enabling me to streamline processes and drive efficiency.

In my previous role as a Regulatory Affairs Coordinator at Contract Pharmaceuticals Limited, I improved submission efficiency by 15% through cross-functional collaboration with teams in R&D, Quality Assurance, and Marketing. This experience honed my skills in compliance documentation for FDA and USDA standards, which I now apply in projects aimed at optimizing workflow, reducing bottlenecks, and enhancing layout efficiency.

As a part of the Riipen project, I am excited to leverage my analytical skills, regulatory expertise, and experience in Lean methodologies to deliver insights that drive measurable improvements in production workflows. My recent projects, including a Six Sigma initiative in a high-volume production environment, focused on maximizing throughput and improving labour efficiency, furthering my commitment to data-driven solutions and sustainable growth in production environments.

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  Riipen Level UP 🚀

  Vancouver, British Columbia, Canada
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  Advanced Manufacturing

  Toronto, Ontario, Canada