At a Glance
- Tasks: Lead the EU regulatory strategy for Class III medical devices and ensure compliance with regulations.
- Company: Join a globally recognised organisation making a difference in healthcare.
- Benefits: Long-term career progression and the chance to work on impactful projects.
- Why this job: Shape the future of medical devices while advancing your career in a dynamic environment.
- Qualifications: Extensive experience in Regulatory Affairs for Class III medical devices and knowledge of EU regulations.
The predicted salary is between 60000 - 80000 £ per year.
Cure Talent is excited to announce a new opportunity for a Regulatory Affairs Manager in Witney, England. This pivotal role involves leading the EU regulatory strategy for a Class III medical device, ensuring compliance with MDR 2017/745, and interacting with global regulatory teams.
The successful candidate will possess extensive experience in Regulatory Affairs within medical devices, particularly for Class III products, and will demonstrate a depth of knowledge in EU regulations.
This role offers significant long-term progression potential in a globally recognized organization.
EU Regulatory Lead for Class III Medical Devices employer: Cure Talent
Cure Talent is an exceptional employer, offering a dynamic work environment in Witney that fosters innovation and collaboration. With a strong commitment to employee development, we provide ample opportunities for growth within the regulatory affairs sector, particularly for those passionate about medical devices. Our inclusive culture and focus on compliance ensure that you will be part of a team that values your expertise and contributions while making a meaningful impact in healthcare.
