- 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
📌 Regulatory Affairs Professional (Bengaluru)
🏢 Caliber Organisation
📍 Bengaluru
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