At a Glance
- Tasks: Lead the EU regulatory strategy for a new Class III medical device.
- Company: Globally recognised organisation with a focus on innovation in healthcare.
- Benefits: Significant responsibility, career progression, and the chance to make a real impact.
- Other info: Dynamic role with opportunities for growth and collaboration across teams.
- Why this job: Shape the future of medical devices and work with top professionals in the field.
- Qualifications: Proven experience in EU regulatory strategies for Class III devices.
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 is pivotal within a globally recognized organization, ensuring alignment across regulatory, clinical, and R&D teams.
The ideal candidate will have proven experience in leading EU regulatory strategies, particularly for Class III devices, coupled with the ability to manage complex timelines and interactions with Notified Bodies. This is a high-impact role that offers significant responsibility and career progression.
EU MDR Lead, Class III Regulatory Affairs Manager in England employer: Cure Talent
Cure Talent is an exceptional employer, offering a dynamic work environment where innovation meets collaboration. With a strong focus on employee growth and development, we provide ample opportunities for career progression within the regulatory affairs sector, particularly in the exciting field of Class III medical devices. Our inclusive culture fosters teamwork and creativity, making it a rewarding place to contribute to impactful healthcare solutions.
