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Job description
Entrada Therapeutics in Boston, MA, is seeking an Associate Director, Analytical Development & Quality Control to lead late-stage AD&QC activities, manage regulatory submissions, and ensure GMP compliance for oligonucleotide programs.
You will collaborate with CMC SMEs, QA, Regulatory, and CDMOs, support IND/IMPD/NDA/MAA filings, and help readiness for inspections, with a US-based remote role requiring periodic travel to the Boston headquarters.
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Worksite address
boston, MA, 02298, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.