CENTERPIECE seeks a Sr Sterilization Validations engineer to lead validation programs in a regulated medical device environment in Baja California. You will develop, implement, and execute validation plans with a strong emphasis on quality and compliance.

You will work closely with operations and quality teams to ensure on-time delivery of validation projects, generate IQ/OQ/PQ protocols and risk assessments, and maintain alignment with 21 CFR 820, ISO 13485, and ISO 11135 requirements.