Associate Director, Analytical Development & QC

Company Name: Entrada Therapeutics

Job Overview

Lead the development, implementation, and improvement of internal QC systems. Manage QC gap analyses and CDMO partnerships for analytical method transfer, qualification, and validation. Oversee QC quality events, including change controls, deviations, and investigations. Partner with internal and external teams, including CRO/CDMOs, for analytical method transfer, qualification, stability programs, and regulatory submissions.

Requirements

• Ph.D. in a relevant science
• 6+ years of GMP experience in biotech/pharma
• Strong knowledge of QC principles
• cGMP experience
• Experience with oligonucleotide analytical methods