Regulatory Affairs Manager

  • Prioritize, devise and govern on product registration and re-certifications for his/her particular product lines;
  • Lobby with a internal health authorities regulating constructive/scientific hurdles to regulations – This should embody superintendence on choice solutions to nation regulatory needs;
  • Supports proposal operations by timely supply of accurate regulatory documents;
  • Establish and say a good operative attribute with informal and local RA peers to benefit certain timely support for request preparation, acquiescence and approval;
  • Serves as regulatory consultant to selling group and supervision regulatory agencies, Communicates with efficient authorities on margin visual actions, commitment etc.
  • Saudi Nationals with during slightest 3-5 years of believe in Regulatory Affairs, preferably within Medical Devices
  • Transferable Iqama for Non-Saudis
  • Fluent in both English and Arabic
  • Sound believe of RA/QA Activities and procedures, documentation, as good as carrying clever relations with POCs within SFDA.
  • Willingness to transport as required.
  • Valid Driver’s License


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