Associate Director, Drug Product QA

Merck is seeking an Associate Director for Drug Product Quality Assurance to establish a robust Quality structure and ensure cGMP conformance across DP operations in Delaware. The role drives regulatory readiness, CAPA programs and continuous improvement for sterile DP manufacturing.

You will lead the DP QA team, oversee batch record review, investigations, and regulatory submissions support, while partnering across functions to maintain the highest product quality.

We are seeking a motivated Associate Director, Drug Product QA
- Hybrid Role to join Merck in Wilmington, DE, United States.

This posting is for the Associate Director, Drug Product QA
- Hybrid Role role at Merck, based in Wilmington, DE, United States.

We are looking to fill the Associate Director, Drug Product QA
- Hybrid Role position at Merck in Wilmington, DE, United States.