Associate Director, Analytical Development & QC

Company Name: Entrada Therapeutics

Job Overview

Lead the development, implementation, and improvement of internal QC systems and manage CDMO partnerships for analytical method transfer, qualification, and validation.

Responsibilities:

• Managing QC quality events
• Authoring SOPs
• Overseeing stability programs
• Supporting regulatory submissions

Requirements:

• Ph.D. or MS in a scientific field
• 6+ years of analytical/QC experience in biotech/pharma under GMP
• Strong knowledge of QC principles, cGMP, and regulatory guidelines