Regulatory and Quality Operations Associate
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I am a detail-oriented and motivated pharmacy graduate currently pursuing a post-graduate certificate in Pharmaceutical Regulatory Affairs and Quality Operations at Seneca College. With a strong background in healthcare and medication safety, I bring hands-on experience in long-term care pharmacy operations, regulatory documentation, and compliance support. I am passionate about drug safety and vigilance, and I am eager to contribute to health product compliance through roles in pharmacovigilance, regulatory affairs, or quality assurance.
I thrive in fast-paced, collaborative environments and am committed to continuous learning and professional growth in the life sciences industry.
Pharmacy graduate with hands-on experience in long-term care and clinical pharmacy environments. Skilled in medication packaging, verification, and distribution processes, with a strong focus on regulatory compliance and patient safety. Previous experience as an intern pharmacist involved counseling, adverse drug reaction monitoring, and inventory management.
Now pursuing specialized training in Pharmaceutical Regulatory Affairs and Quality Operations, with growing expertise in Good Manufacturing Practices (GMP), pharmacovigilance, and regulatory documentation. Proven ability to work in fast-paced, detail-sensitive roles while contributing to team efficiency and quality standards.
Currently pursuing a Post-Graduate Certificate in Pharmaceutical Regulatory Affairs and Quality Operations at Seneca College, Toronto, ON (Expected Completion: December 2025). The program provides in-depth training in regulatory compliance, pharmacovigilance, quality assurance, clinical research, and Good Manufacturing Practices (GMP), with a focus on Health Canada, FDA, and international regulatory frameworks. Coursework includes hands-on assignments in regulatory submissions, SOP development, quality systems, and vigilance reporting