Process Validation Engineer – Hybrid Role in Medical Devices

KeyMed (Medical & Industrial Equipment) Ltd. (OKM) is seeking a Process Validation Engineer to lead process validation activities in a manufacturing environment.

You will develop the Site Master Validation Plan, create risk-based protocols, and execute validation tasks while supporting other engineers and mentoring colleagues. The role requires understanding of FDA 21 CFR Part 820, ISO 13485:2016, and DOE-based validation methods.

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