I have 5 years of experience in the pharmaceutical industry in the areas of regulatory and quality. In my most recent role at GSK, I was responsible for preparing and publishing regulatory submissions and managing lot releases for various products, including vaccines, oncology, cardiovascular, and HIV products.I demonstrate collaborative problem-solving, organizational, and time management skills to coordinate with multiple stakeholders, such as Health Canada, Quality, Supply, Marketing, and Pharmacovigilance to ensure compliance, and timely regulatory deliverables.I am motivated by the opportunity to contribute to the health and well-being of people around the world and to bring diverse perspectives and experiences to a regulatory affairs team.