EU Regulatory Affairs Lead – Hybrid & Lifecycle Strategy
Listed on 2026-10-13
-
Pharmaceutical
Regulatory Compliance Specialist
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.
The following opportunity is for a EU Regulatory Affairs Lead – Hybrid Work & Lifecycle Strategy with Amgen.
Join Amgen and contribute to our ongoing work.
Take a moment to read everything above and see whether this role is right for you.
This posting is for the EU Regulatory Affairs Lead – Hybrid Work & Lifecycle Strategy role at Amgen, based in Uxbridge, England, United Kingdom.
We are looking to fill the EU Regulatory Affairs Lead – Hybrid Work & Lifecycle Strategy position at Amgen in Uxbridge, England, United Kingdom.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).