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About Company

ResMed’s products must comply with regulatory requirements applicable to medical devices for the markets in which they are sold. This includes compliance with the Food and Drug Administration (FDA) in the United States, the relevant competent authorities in Europe, and the Therapeutic Goods Administration (TGA) in Australia, as well as international standards such as ISO 13485. ResMed products are marketed based on a reputation of high-quality standards for workmanship, performance, and reliability.

Position Name :

Regulatory Affairs Administrative Assistant

Organization :



B.Pharm, M.Pharm, Msc, BSc


1 to 2 Years


25,000 - 35,000 /month



A Regulatory Affairs Administrative Assistant provides essential support to regulatory affairs professionals in managing compliance, documentation, and administrative processes. They play a crucial role in ensuring smooth operations within the regulatory department.

Responsibilities and Accountabilities

  • Document Management: Assist in preparing, compiling, and maintaining regulatory documentation, including submissions, forms, reports, and records.
  • Communication: Handle administrative requests and queries related to regulatory matters.
  • Meeting Coordination: Schedule and organize meetings, including taking detailed minutes during regulatory discussions.
  • Filing System: Develop and maintain an organized filing system for regulatory documents, including updates to tracking systems.
  • Policy Updates: Assist in updating and maintaining policies and procedures related to regulatory affairs.
  • Liaison: Act as a point of contact for internal and external stakeholders regarding regulatory inquiries.

Application Link

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