Manage and administer CRISPR's Quality Management System, focusing on deviation, change control, and CAPA processes while ensuring compliance and enhancing procedures.

The Associate Director of Pharmacovigilance Operations will oversee global case processing, safety reporting, and vendor management in clinical programs, ensuring compliance and effective safety operations.

The Senior Scientist leads analytical method development for mRNA therapeutics, collaborating with internal teams and external laboratories, while ensuring regulatory compliance and mentoring junior scientists.

The Senior Manager/Associate Director of Business Development will facilitate partnerships, perform strategic analysis, and manage existing deals in biopharma.