I’m Victoria Lee Ostinelli, a Regulatory Affairs and Life Sciences professional based in Switzerland, with experience turning complex regulatory requirements into clear product safety and compliance paths. I’ve supported delivery across Swiss, EU, and global environments by translating documentation needs into practical workflows for teams across regulatory, quality, clinical, technical, legal, and commercial functions—especially for medtech-adjacent digital health solutions.
Across my roles at companies and international organizations, I’ve led risk-mitigated launches, strengthened audit readiness, and helped build scalable product life cycle approaches. I’m currently deepening my regulatory expertise through a CAS program in Regulatory Affairs and Life Sciences at the University of Bern, and I bring a strong blend of stakeholder leadership, GMP/ISO-aligned thinking, and technical understanding to help organizations stay compliant while delivering meaningful health impact.
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