PQE Group is seeking an experienced Quality Assurance & Regulatory Affairs professional to support a Medical Device organization. You will act as an extension of the manufacturer's quality and regulatory team, ensuring compliance with EU MDR 2017/745 and ISO 13485/9001/14001.The role involves hands-on quality and regulatory activities across audits, CAPAs, deviations, and post-market surveillance, with opportunities to collaborate on international projects and product registrations.#J-18808-Ljbffr
📌 Senior Qara Specialist – Medtech Compliance & Mdr Lead (Madrid)
🏢 Pqe Group
📍 Madrid
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