About the role

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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JOB OVERVIEW

Experience level

Lead

Location

East Boston, MA

Occupation

Regulatory Affairs Managers

Industry

Research and Development in Biotechnology (except Nanobiotechnology)

Posted

yesterday

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