At a Glance
- Tasks: Ensure compliance with UK and EU regulations for medical devices and manage technical documentation.
- Company: Join a leading medical device manufacturer in Worcestershire with a focus on quality.
- Benefits: Competitive salary, career development opportunities, and a supportive team environment.
- Other info: Be part of a dynamic team dedicated to innovation and compliance.
- Why this job: Make a difference in healthcare by ensuring the safety and efficacy of medical devices.
- 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 in England 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.