At a Glance
- Tasks: Lead the EU regulatory strategy for a groundbreaking Class III medical device.
- Company: Cure Talent, a forward-thinking company in the medical device sector.
- Benefits: Long-term career progression and a dynamic work environment.
- Other info: Collaborate with global teams in a structured organisation.
- Why this job: Make a significant impact in healthcare by shaping regulatory strategies.
- Qualifications: Proven experience in regulatory affairs and knowledge of EU MDR 2017/745.
The predicted salary is between 60000 - 80000 £ per year.
Cure Talent is seeking a Regulatory Affairs Manager to lead the EU regulatory strategy for a new Class III medical device. This role requires proven experience in regulatory affairs within structured global organizations and expertise in navigating EU MDR 2017/745.
The successful candidate will oversee regulatory project management, ensuring successful alignment between global regulatory, clinical, and R&D teams. This high-impact position offers long-term progression opportunities in a dynamic environment.
EU Regulatory Strategy Lead for Class III Medical Devices in England employer: Cure Talent
Cure Talent is an exceptional employer, offering a vibrant work culture that fosters collaboration and innovation in the medical device sector. With a strong commitment to employee development, we provide ample opportunities for growth and advancement, ensuring that our team members thrive in their careers while making a meaningful impact on healthcare. Located in a dynamic environment, we encourage a balance between professional challenges and personal well-being, making us an attractive choice for those seeking rewarding employment.
