Senior Regulatory Affairs Manager – Med Devices & IVDs (EU/UK) in Cambourne

Senior Regulatory Affairs Manager – Med Devices & IVDs (EU/UK) in Cambourne

Cambourne Full-Time 63000 - 77000 Β£ / year (est.) No working from home possible
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At a Glance

  • Tasks: Lead regulatory activities for medical devices and IVDs, ensuring compliance with EU MDR/IVDR.
  • Company: TOGL (Holdings) Limited, a forward-thinking company in Cambridge.
  • Benefits: Competitive salary, career advancement, and the chance to make a difference in healthcare.
  • Other info: Opportunity to liaise with international markets and Notified Bodies.
  • Why this job: Shape the future of medical devices while working with a dynamic team.
  • Qualifications: Degree in Biomedical Science and extensive regulatory experience required.

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

TOGL (Holdings) Limited, Cambridge, seeks a proactive Regulatory Affairs Manager to lead regulatory activities for medical devices and IVDs, including SaMD. You will develop Technical Documentation per EU MDR/IVDR, support lifecycle management, and liaise with Notified Bodies and authorities across EU, UK and international markets.

The role requires a degree in Biomedical Science or related field and extensive regulatory experience, with strong English communication and cross-functional skills.

Senior Regulatory Affairs Manager – Med Devices & IVDs (EU/UK) in Cambourne employer: TOGL (Holdings) Limited

TOGL (Holdings) Limited is an excellent employer, offering a dynamic work environment where precision and organisation are valued. Employees benefit from a collaborative culture that fosters professional growth and development, alongside opportunities to contribute meaningfully to impactful clinical research. Located in a state-of-the-art facility, the company prioritises employee well-being and provides resources to ensure a fulfilling work experience.

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Contact Details:

TOGL (Holdings) Limited Recruitment Team

We think you need these skills to ace Senior Regulatory Affairs Manager – Med Devices & IVDs (EU/UK) in Cambourne

Regulatory Affairs
Technical Documentation
EU MDR
IVDR
SaMD
Lifecycle Management
Liaising with Notified Bodies