I am a Qualified Person (QP) and Technical Director with extensive experience in Advanced Therapy Medicinal Products (ATMPs), GMP manufacturing, and quality assurance. At Hospital Sant Joan de Déu, I have been part of the team driving the launch and development of the Advanced Therapies Platform, establishing GMP-compliant infrastructure, quality systems, and manufacturing processes for cell and gene therapy products.
Over more than 15 years, I have combined a strong scientific background (PhD in Biochemistry and Molecular Biology) with hands-on expertise in regulatory compliance, batch release, deviation management, CAPA, and internal audits. My career spans CAR-T cell manufacturing, viral vector production, and the implementation of robust Quality Management Systems (QMS) under EMA regulations.
Key strengths include:
- Leading multidisciplinary teams to deliver ATMP projects under GMP
- Translating cutting-edge research into clinical-grade manufacturing processes
- Managing inspections, audits, and regulatory submissions
- Driving continuous improvement and operational excellence in cell and gene therapy production
I am passionate about advancing innovative therapies from lab to patient, and I enjoy collaborating with partners who share the vision of bringing transformative cell and gene therapies to the clinic. If you are interested in exploring collaboration or discussing opportunities in ATMP manufacturing, quality, or regulatory leadership, let’s connect.