Director, Regulatory Affairs (digital Medical Devices)

Novartis

London, United Kingdom
On-site
Significant experience in digital device industry
Lead global digital device submission activities
Ability to work independently with global teams
This role drives regulatory direction across development, registration, and post-approval

Job Summary

  • This role drives regulatory direction across development, registration, and post-approval.
  • You will ensure timely, compliant decisions that balance patient safety and business needs.
  • Novartis is committed to building an outstanding, inclusive work environment.

Matching Summary

This role drives regulatory direction across development, registration, and post-approval.

Skills & Requirements

Must-have

  • Significant experience in digital device industry
  • Lead global digital device submission activities
  • Ability to work independently with global teams

Nice-to-have

  • Knowledge sharing within Regulatory Affairs
  • Experience in regulatory health authority interactions
  • Ability to critically evaluate scientific data

Key Requirements

  • Science Degree or equivalent
  • Experience with digital device regulatory submission processes
  • Demonstrated practical experience in regulatory affairs

Work Rights

Not specified

Tailored Resume

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