EU Regulatory Affairs Lead – Hybrid Work & Lifecycle Strategy

Amgen Inc. in the United Kingdom (Uxbridge/Cambridge hybrid) seeks an EU Regulatory Affairs Manager to lead submissions for clinical trials and marketed products.

You will craft regional regulatory strategies, provide guidance for regulatory documents, and ensure compliance with EU requirements across the product lifecycle. The role requires experience with regulatory procedures (scientific advice, orphan apps, PIP, MA) and strong communication.

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