Specialist, Regulatory Affairs

Mundipharma

  • Riyadh
  • Permanent
  • Full-time
  • 1 month ago
ARA-P1-10Responsible for dossier compilation and submission • Responsible for ensuring compliant life cycle management in compliance with market regulations • Manage local Labeling and AWs creation and submission • Maintain the regulatory processes within the department, including assist with the development and implementation of regulatory procedures and SOP, • Manage Communication with regulatory agencies or related interfaceAdditional Job Description:Primary Location: SA RiyadhJob Posting Date: 2025-07-16Job Type: Permanent

Mundipharma

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