Veronica Bosa

Background

About Veronica Bosa

Clinical Pharmacy graduate with over 4years of professional experience in the pharmaceutical industry. Quality Assurance professional with solid experience across Quality Control, Quality Systems, and Compliance in the pharmaceutical industry. Currently, as a QA Compliance Specialist at Novartis, I am responsible for the approval of analytical documentation and for providing QA oversight of LIMS activities, ensuring data integrity and GMP compliance. Previously, as a Quality Systems & Compliance Specialist at STADA, I managed product quality specifications in alignment with registration dossiers, maintained master data and also static data in SAP and LIMS, creating and approved inspection and testing plans. I closely collaborated with the QC department to ensure documentation consistency and GMP standards and also with Production area to ensure sample plans for every PO realeased. Earlier, as a QC Analyst at Novartis, I performed impurity, assay, and residual solvent testing using HPLC, UPLC, and GC, gaining strong technical expertise in analytical chemistry. I am passionate about ensuring data integrity, maintaining high-quality standards, and continuously improving pharmaceutical quality systems. Quality Systems & Compliance, where I actively support the development and maintenance of quality systems in accordance with GMP standards and product dossiers.