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  3. Victoria Quiroga, MSc.

Victoria as Associate Director in Chemistry, Manufacturing, and Control (CMC), specializes in authoring and reviewing Quality Modules for global regulatory submissions, as well as briefing documents for Agency interactions. Her expertise focuses on Cell and Gene Therapy Products, with experience in advanced technologies such as gene editing, mRNA-based therapies, CAR-T cells, viral vectors, and tissue engineering. With over ten years of experience, she has held leadership roles in Quality Assurance and Regulatory Affairs, showcasing her strong background in ensuring compliance and quality standards.

Insights by Victoria Quiroga, MSc.