Associate Director, Analytical Development & QC

Company Name: Entrada Therapeutics

Job Overview

The Associate Director, Analytical Development & QC will lead the development, implementation, and improvement of internal QC systems and manage QC quality events (e.g., change controls, deviations, investigations).

Responsibilities

• Oversee CDMO partnerships for analytical method transfer, qualification, and validation.
• Manage stability programs and reference standard management.
• Conduct proactive QC gap analysis.
• Collaborate across functional teams.

Requirements

• Ph.D. or MS in a relevant scientific field.
• 6+ years of analytical/QC experience in a GMP biotech/pharma environment.
• Strong knowledge of QC principles.
• Familiarity with cGMP regulations.