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Regulatory Affairs Professional

Caliber Organisation

RemoteFull timeMid levelPosted today
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About the role

  • Regulatory support for medical device software and software-enabled systems
  • Preparation, review, and maintenance of regulatory documentation
  • Support for regulatory submissions and change management activities
  • Interpretation and application of global regulatory requirements
  • Collaboration with internal Philips project teams, software leads, and quality teams
  • Ongoing regulatory guidance throughout the product lifecycle

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