With 2 years in the pharmaceutical industry, I have excelled as a Quality professional and lecturer coordinator, boasting a solid educational background in Chemistry. Proficient in eCTD submissions, SOP crafting, and advanced scientific and GLP-compliant LAB practices, I understand Canadian and international drug regulations. My expertise extends to GMP, GLP, and GDP, thriving in fast-paced environments. As a dedicated Regulatory Affairs-focused university student, I prioritize prompt project completion and continual adaptation. A team-oriented collaborator, having developed a deep understanding of industry-standard software, hardware, and network configurations. Proficient in PHARMASUIT, PHARMACLOUD, MS Office, Adobe, Outlook, and various professional tools.