Flex is seeking a Process Validation Engineer (Medical Devices) to support validation activities in Juarez South. You will lead IQ/OQ/PQ and TMV studies, develop validation protocols, and ensure compliance with FDA and ISO 13485 standards.
The role collaborates with Quality, Manufacturing, Regulatory Affairs, and R&D; to drive product quality and regulatory readiness. We value a Bachelor’s degree in engineering and 3–5 years in regulated environments, with strong English skills and a focus on
📌 Medical Device Process Validation Engineer – IQ/OQ/PQ Lead (Sonora)
🏢 Flex
📍 Sonora
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