Validation Engineer I - Medical Devices (IQ/OQ, GMP)

A consulting and staffing solutions company is seeking a Validation Engineer I in Santa Clara, CA. This role requires at least 1 year of validation experience in a medical device or pharmaceutical industry. Responsibilities include developing qualification matrices, preparing and executing IQ/OQ protocols, and ensuring compliance with FDA regulations. The position offers a contract term of 6 months with possible extensions and is backed by competitive benefits including medical, dental, vision, and life insurance. #J-18808-Ljbffr