About this opportunity
CRISPR Therapeutics lists this Regulatory Affairs CMC Lead – Gene Therapy (Hybrid) opportunity in boston, Massachusetts. Review the employer’s description below for duties, qualifications and application requirements.
Job description
CRISPR Therapeutics, based in Boston, is seeking an Associate Director for Regulatory Affairs CMC to oversee regulatory strategies for innovative gene therapies. This leadership role requires extensive experience in CMC regulatory requirements for biologics and gene therapies.
The ideal candidate will have over 12 years of regulatory experience and a strong understanding of FDA and EMA guidelines, with a proven record of successful submissions. This position promotes a collaborative work environment with flexible remote options.
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Worksite address
boston, MA, 02298, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.