Philips Regulatory Affairs Specialist in Bangalore, India

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  • Be part of Project Core Team

  • Communicate regulatory project status/issues to Q&R organization and stakeholdersResponsible and accountable for creating and driving the execution of the project regulatory plan

  • Manage worldwide product registrations

  • Ensure project activities are complete to support compliance claims for MDD essential requirements

  • Drive FDA/ NMPA/CFDA submissions

  • Assist Philips country offices and/or dealers in obtaining the product registrations outside of North America and the European Union

  • Engage Clinical Marketing Representative on project deliverables related to clinical agreements and Clinical Readiness Reviews

  • Manage local Regulatory requirements