Teams at BioMarin Pharmaceutical Inc.

Leads Good Pharmacovigilance Practice compliance within Global Quality, advising stakeholders on regulations, policies, audits, inspection readiness, risk mitigation, and quality systems. Performs GVP audits, supports regulatory inspections and mock readiness, contributes to PSMF and REMS compliance, improves audit programs, and mentors junior staff. Requires extensive pharmacovigilance quality and compliance experience, regulatory knowledge, audit leadership, strong communication, and strategic decision-making.

Conducts quantitative genomics and statistical genetics analyses integrating human genetics, sequencing, EHR/claims, real-world evidence, and AI/ML data. The role defines patient populations, biomarkers, disease segments, and diagnostic pathways; manages external collaborations; evaluates data providers and cohorts; supports clinical and commercial patient-finding strategies; informs portfolio prioritization; and communicates evidence-based recommendations across scientific and business stakeholders.