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.
#J-18808-Ljbffr
EU Regulatory Affairs Lead – Hybrid Work & Lifecycle Strategy in Uxbridge employer: Amgen
At Amgen, we pride ourselves on being a leading biotechnology company that prioritises the well-being and growth of our employees. As an EU Regulatory Affairs Manager, you will be part of a diverse and inclusive team dedicated to serving patients, with ample opportunities for professional development and a generous Total Rewards Plan. With flexible working arrangements from our offices in Cambridge, Uxbridge, or Lisbon, you can enjoy a fulfilling career while maintaining a healthy work-life balance.
