Validation Engineer - Medical Devices; IQ​/OQ, GMP

Position: 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.
We are seeking a motivated Validation Engineer I
- Medical Devices (IQ/OQ, GMP) to join BEPC Inc.

- Business Excellence Professional Consulting in Santa Clara, CA, United States. We would love to welcome a new Validation Engineer I
- Medical Devices (IQ/OQ, GMP) to our organisation in Santa Clara, CA, United States. For the Validation Engineer I
- Medical Devices (IQ/OQ, GMP) position at BEPC Inc.

- Business Excellence Professional Consulting, we are reviewing applications now.