Amgen is seeking an EU Regulatory Affairs Manager to lead regulatory submissions and strategy for clinical trials and marketed products across Europe. You will collaborate with global teams to ensure compliance with EU requirements and optimize product development timelines.
The role involves planning submissions, guiding regional regulatory activities, and staying abreast of evolving legislation, with responsibility for lifecycle management and label negotiations.
#J-18808-LjbffrEU Regulatory Affairs Lead — Remote/Hybrid in Uxbridge employer: Amgen SA
Amgen SA in Cambridge is an exceptional employer, offering a dynamic work culture that fosters innovation and collaboration. With a strong focus on employee growth, you will have access to competitive rewards and flexible working conditions, making it an ideal environment for those looking to make a meaningful impact in the field of rare and inflammatory diseases.
