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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EU Regulatory Affairs Lead – Hybrid Work & Lifecycle Strategy in Uxbridge employer: Amgen Inc. (IR)
Amgen is an exceptional employer, offering a dynamic work environment where innovation and collaboration thrive. With a strong commitment to employee growth, Amgen provides numerous opportunities for professional development within a diverse and inclusive community. Located in vibrant cities like Cambridge, Uxbridge, or Lisbon, employees enjoy flexible working arrangements and a generous Total Rewards Plan that prioritises health, work/life balance, and career advancement.
