DHF Quality Systems Engineer – Medical Devices

Enhanced Compliance Inc. is seeking a DHF Engineer to join the Regulatory Compliance Work Stream. You will establish Quality Systems with a focus on 21 CFR 820 and ISO 13485, working with clients in the life sciences sector to ensure robust compliance.

You will lead quality-system projects, develop SOPs and templates, audit programs, and map regulatory requirements to QSI documents. Strong communication, auditing experience, and SME-level knowledge of ISO 9001/13485 are essential.

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