Regulatory Lead, Class IIa Medical Devices & Digital Health in London

Regulatory Lead, Class IIa Medical Devices & Digital Health in London

London Full-Time 60000 - 80000 £ / year (est.) No working from home possible
Beam

At a Glance

  • Tasks: Lead regulatory compliance for innovative healthcare products and drive Class IIa certification.
  • Company: Join Beam, a forward-thinking company in digital health.
  • Benefits: Competitive salary, flexible working options, and opportunities for professional growth.
  • Other info: Collaborative environment with a focus on innovation and impact.
  • Why this job: Make a real difference in healthcare by shaping regulatory pathways for cutting-edge technology.
  • Qualifications: Experience in regulatory affairs and a passion for digital health.

The predicted salary is between 60000 - 80000 £ per year.

Beam is seeking a Quality & Regulatory Affairs Lead - Digital Health to own clinical compliance and regulation across our healthcare products.

In this high‑ownership role you will drive towards Class IIa medical device certification and serve as the day‑to‑day contact for cross‑functional teams.

You’ll shape the healthcare regulatory roadmap, manage DCB documentation, and engage MHRA/DHSC to keep us aligned with international standards.

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Regulatory Lead, Class IIa Medical Devices & Digital Health in London employer: Beam

At Beam, we pride ourselves on being an exceptional employer, offering a dynamic remote work environment that fosters innovation and collaboration. Our culture is built on meaningful work that addresses critical social issues, providing employees with opportunities for professional growth and the chance to make a real impact. Join us and be part of a passionate team dedicated to leveraging technology and AI for positive change in the world.

Beam

Contact Details:

Beam Recruitment Team

We think you need these skills to ace Regulatory Lead, Class IIa Medical Devices & Digital Health in London

Clinical Compliance
Regulatory Affairs
Class IIa Medical Device Certification
Cross-Functional Team Collaboration
Healthcare Regulatory Roadmap Development
DCB Documentation Management
Engagement with MHRA