Jasmina Stevanovic

Background

About Jasmina Stevanovic

Dynamic, detail-oriented pharmaceutical professional, experienced in various aspects of product quality with a proven track record of outstanding results and commitment to excellence. This array of expertise, grounded in a robust understanding of GMP and regulatory guidelines, along with aim for continuous improvement, facilitates transitioning to new challenges. • 13 years of experience in pharmaceutical Quality and R&D • 7 years in GMP environment • Pharmaceutical Quality Assurance Post-Graduate Certificate • Comprehensive knowledge of Canadian GMP, cGMP, Health Canada, FDA, ICH guidelines and regulations and WHMIS • Extensive experience in GMP Documents review • Experience in LIR, CCR and CAPA • In-depth knowledge change control, deviations, validation, audits, monthly reports and regulatory submissions for Health Canada and the FDA • Experience with creation, revision, and review of master batch records, SOPs and stability reports and ensured completeness and accuracy of information • Energetic, work well under pressure • Superior attention to accuracy and detail while coordinating multiple projects simultaneously • Effectively recognized, reported and investigated OOS and OOT results • Robust knowledge and understanding of analytical instrumentation HPLC/UPLC, GC, UV/Vis, IR, KF and auto-titrator, among other instrumentation • Able to exercise flexibility, initiative, strong ethics and sound judgment in handling confidential materials, identifying and resolving issues • Outstanding written and verbal communication skills necessary to maintain positive working relationships • Able to work effectively in a team-based environment as well as independently • Highly proficient in Microsoft Office suite, Adobe Acrobat, SAP, Empower, among other laboratory software