Regulatory Affairs Specialist, Medical Devices

Regulatory Affairs Specialist, Medical Devices

Full-Time 63000 - 77000 Β£ / year (est.) No working from home possible
Cure Talent

At a Glance

  • Tasks: Ensure compliance with UK and EU regulations for medical devices and manage technical documentation.
  • Company: Leading medical device manufacturer in Worcestershire with a focus on quality and innovation.
  • Benefits: Competitive salary, supportive team environment, and opportunities for professional growth.
  • Other info: Exciting opportunity to work with cutting-edge medical technologies.
  • Why this job: Join a dynamic team and make a difference in the medical device industry.
  • Qualifications: Proven experience in Regulatory Affairs and strong knowledge of relevant regulations.

The predicted salary is between 63000 - 77000 Β£ per year.

Cure Talent are partnered with a medical device manufacturer in Worcestershire seeking a Regulatory Affairs Specialist to join the Quality & Regulatory team in Bromsgrove. You will ensure ongoing compliance with UK MDR and EU MDR, manage technical documentation, regulatory submissions and liaise with MHRA and Notified Bodies throughout the product lifecycle.

You should have proven Regulatory Affairs experience in medical devices, with strong knowledge of UK MDR, EU MDR, UKCA and ISO 13485.

Regulatory Affairs Specialist, 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.

Cure Talent

Contact Details:

Cure Talent Recruitment Team

We think you need these skills to ace Regulatory Affairs Specialist, Medical Devices

Regulatory Affairs Experience
Knowledge of UK MDR
Knowledge of EU MDR
Knowledge of UKCA
Knowledge of ISO 13485
Technical Documentation Management
Regulatory Submissions