Parexel is seeking an experienced Regulatory Affairs professional to lead regulatory strategy for medical devices and drug-device combinations across Europe. The role can be home or office based in various European locations.
You will develop global regulatory strategies, interact with health authorities and notified bodies, and coordinate submissions while collaborating with CMC and QA teams. Fluent English is required.
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📌 Regulatory Affairs Lead: Medical Devices & Combo Products EU (Milano)
🏢 Parexel
📍 Milano
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