GMP Professional with Regulatory and Quality Experience at Teva Pharmaceutical
Toronto, ON
Pharmaceutical GMP professional with 3+ years of experience at Teva Pharmaceuticals, combined with a 4.0 GPA Graduate Certificate in Pharmaceutical Regulatory Affairs & Quality Operations (Seneca Polytechnic, 2025) & Project Management. Hands-on contributor to global regulatory submissions knowledge management projects alongside quality systems role in GMP Teir-1 manufacturing. Proven in controlled document management, deviation investigation, CAPA execution, and audit readiness under Health Canada and FDA standards.
Teva Pharmaceuticals
2023 - PresentExecute quality review of high-volume GMP production of solid dosage forms with 100% adherence to Master Batch Records and GMP standards; perform In-Process Controls including Karl Fischer titration and physical QC testing. Maintain batch record documentation ensuring 100% ALCOA++ compliance.
Teva Pharmaceuticals
2023 - 2023Maintained 100% ALCOA+ documentation compliance across logbooks and batch records; executed GMP production of solid dosage forms in strict adherence to Master Batch Records, ensuring compliance with Health Canada and FDA standards.
Ontario Graduate Certificate in Pharmaceutical Regulatory Affairs & Quality Operations
2024 - 2025Graduate Certificate in Project Management
2021 - 2021Bachelor of Science in Chemistry
2012 - 2015Teva Pharmaceutical
2025 - PresentOntario, CanadaReduce no. of review letters; Expedite Approvals; Learning from products (FTR approach); Generate One-stop pool of HAQs. Utilize Veeva RIM (GRIDS) to gather data in excel (e.g. Issue/Start Date, Received Date, Correspondence Scope, Type of Letter). Also, identify Product Family, Application, Regulatory Objectives Submissions type & Country.
Teva Pharmaceutical
2025 - PresentOntario, CanadaUtilize Veeva RIM (GRIDS) to identify and standardize data & metadata requirements for global regulatory submissions to de-risk Agency requests for information (RFI) for early phase submissions; provide predictability & visibility; promote right first time; build consistency across programs; enhance collaboration with R&D teams.