Regulatory Affairs CMC Lead – Gene Therapy Programs

CRISPR Therapeutics, Inc. is seeking an Associate Director, Regulatory Affairs CMC to lead regulatory CMC efforts for a portfolio of gene-based medicines.

You will collaborate with cross-functional teams and partners to devise innovative regulatory strategies while coordinating with contract manufacturers and health authorities worldwide. Reporting to the Head of Regulatory Affairs, you will manage complex CMC topics, prepare high-quality submissions, and guide global teams through INDs, CTAs,