GMP CSV Engineer — Validation & MES Specialist

A leading contract research organization in Bothell is seeking an Entry-Level Validation Specialist responsible for the preparation and execution of test documentation for GMP computerized systems.

The role requires an excellent understanding of regulatory requirements and validation methodologies, with responsibilities including documentation review and validation of automated systems.

This contract position offers an opportunity to work in a dynamic pharmaceutical manufacturing environment.#J-18808-Ljbffr