Experienced Ra Professional Lifecycle Submission

Johnson & Johnson Johnson & Johnson · Pharma · Cairo, Egypt

This role is for an Experienced RA Professional in Lifecycle Submissions within Johnson & Johnson's Innovative Medicine division, based in Cairo, Egypt. The primary focus is on coordinating and executing lifecycle management procedures for pharmaceutical products, ensuring timely submissions, implementation of changes, and database updates in compliance with country-specific requirements and health authority approvals. The role involves strategic planning for submissions, preparing documentation, and acting as a Subject Matter Expert for regulatory affairs.

What you'd actually do

  1. Perform lifecycle management activities per established processes and country-specific requirements.
  2. Propose strategy and timeline for National Procedure (NP) to the LOC.
  3. Prepare submission-ready documents/dossier(s) and ensure timely submission of high-quality (response) dossier.
  4. Process Health Authority (HA) approvals to initiate post-approval activities promptly.
  5. Ensure timely update of databases throughout lifecycle management.

Skills

Required

  • Arabic and English knowledge
  • Pharmacist bachelor’s degree
  • Minimum of 3 years of Regulatory Affairs experience within Emerging Markets
  • Works under general supervision to contribute to projects and tasks
  • Individual contributor who performs more complex assignments and contributes to projects and processes within their area of responsibility
  • Applies general knowledge and understanding of principles and practices to address problems