At a Glance
- Tasks: Lead EU regulatory strategy for a new Class III medical device and manage project leadership.
- Company: Global medical device organisation with a focus on innovation.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Join a dynamic team within a large international function.
- Why this job: Make a significant impact in the medical field by ensuring compliance and safety.
- Qualifications: Experience in regulatory affairs and strong project management skills.
The predicted salary is between 60000 - 80000 £ per year.
Cure Talent are delighted to partner with a global medical device organisation to recruit a Regulatory Affairs Manager who will lead the EU regulatory strategy for a new Class III medical device under MDR 2017/745. This role focuses on regulatory project leadership within a large, international function.
You will define approval pathways, lead Notified Body interactions, and collaborate with R&D, Clinical Affairs, and global Regulatory teams to ensure timely submissions and compliant.
EU MDR Class III Regulatory Lead – Medical Devices employer: Cure Talent
Join a dynamic and innovative medical device manufacturer in Slough, where your role as Procurement Manager will not only enhance your career but also contribute to meaningful healthcare solutions. With a strong focus on employee development, a collaborative work culture, and the opportunity to manage significant procurement budgets, this position offers a unique chance to make a real impact while enjoying a supportive environment that values growth and excellence.
