At a Glance
- Tasks: Manage regulatory strategies for Oncology and General Medicine across Europe.
- Company: Join Amgen, a leading biotechnology company dedicated to improving lives.
- Benefits: Attractive salary, health benefits, and opportunities for professional growth.
- Other info: Dynamic work environment with a focus on collaboration and impact.
- Why this job: Play a crucial role in bringing innovative therapies to patients in need.
- Qualifications: Experience in regulatory affairs and strong communication skills required.
The predicted salary is between 60000 - 80000 £ per year.
Amgen is seeking a Regulatory Affairs Manager to support Oncology or General Medicine teams across Europe, with regulatory responsibilities in Portugal and the United Kingdom.
You will ensure license approvals for trials and marketed products, and guide regional regulatory strategies while engaging with global plans.
The role covers submissions planning, regulatory guidance, and label negotiations, with a focus on enabling efficient product development and timely approvals in the region.
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Regulatory Affairs Manager, Europe – Oncology/Med in Uxbridge employer: Amgen
Amgen in Uxbridge is an exceptional employer, offering a dynamic work culture that prioritises innovation and collaboration in the biopharmaceutical sector. Employees benefit from comprehensive professional development opportunities, competitive compensation, and a commitment to quality and compliance that empowers them to make a meaningful impact on clinical trials. With a focus on employee well-being and a supportive environment, Amgen stands out as a rewarding place to advance your career.
