About this opportunity
Alnylam Pharmaceuticals lists this Regulatory Affairs CMC Lead for Biologics & RNAi Therapies opportunity in cambridge, Massachusetts. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Alnylam Pharmaceuticals is seeking an Associate Director of Regulatory Affairs CMC Development to shape global CMC regulatory strategies for development-stage programs, with emphasis on oligonucleotide-based modalities.
The role bridges Research, Development, and Regulatory Sciences, requiring strong communication and strategic thinking. This hybrid position is based in Cambridge, MA or Philadelphia, PA, offering a comprehensive benefits package.
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Worksite address
cambridge, MA, 02140, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.