Description
The role leads the commercialization of field-successful vector-control compounds through WHO engagement, national regulatory approvals, market access, partnerships, and product-readiness activities. Responsibilities include advancing WHO prequalification and country submissions, closing evidence and product-readiness gaps, resolving manufacturing, supply, distribution, and procurement barriers, and owning commercialization plans, milestones, costs, and partnerships. The position is full-time and in-office in Emeryville, California, requires international and site travel, and offers equity compensation.
