Regulatory Affairs Associate
Toronto, Ontario
Detail-oriented Regulatory Affairs professional with 3 years of experience in Good Manufacturing Practice (GMP) regulated pharmaceutical environments. Demonstrates expertise in collaborating with multidisciplinary teams to ensure the timely and compliant preparation of regulatory documentation for 300+ products.
Infrastructure for Information Inc (i4i.com)
2025 - 2025Supported regulatory operations for 300+ pharmaceutical products by preparing compliant regulatory documentation packages for 45+ global manufacturers.
Contract Pharmaceuticals Limited
2022 - 2024Ensured seamless GMP compliance across the full production lifecycle for Health Canada and FDA-regulated products.
Deciem
2021 - 2022Ensured full compliance with GMP and packaging quality standards by conducting detailed batch record reviews and in-process inspections.
Toxicology Lab, ETH Zurich
2018 - 2020Performed analytical testing using HPLC and chromatography techniques to support chemistry research and method development initiatives.
Certificate in Data Science
2023 - 2024Post Graduate in Pharmaceutical Regulatory Affairs & Quality Operations
2023 - 2025Bachelor of Science in Chemistry
2020 - 2024PG Certificate in Business Administration
2019 - 2021Master of Sciences in Nutrition and Health
2018 - 2020Master of Sciences in Chemistry & Business Information System
2015 - 2017RAPS
2026 - Present