Regulatory Affairs Lifecycle Submissions Specialist (18‑month contract)

About the role

Johnson & Johnson is seeking an experienced Regulatory Affairs professional to lead lifecycle submission activities for its Innovative Medicine portfolio. This 18‑month fixed‑term position will be based in Cairo, Egypt; Cape Town, South Africa; or Casablanca, Morocco, and will work within the Cross‑Regional Operations & Strategic Support (C‑ROSS) team.

Key responsibilities

• Coordinate end‑to‑end lifecycle management procedures for product registrations and changes.
• Prepare and submit regulatory dossiers, ensuring compliance with regional and global requirements.
• Implement approved changes in applicable databases and manage associated artwork updates.
• Conduct routine risk assessments and develop mitigation processes.
• Support cost‑effective, results‑based programs and innovative regulatory initiatives.

Required profile

• Established individual contributor with experience in regulatory affairs lifecycle submissions.
• Ability to work under moderate supervision and collaborate across regional and global teams.
• Strong understanding of Johnson & Johnson’s Credo and Leadership Imperatives.
• Excellent written and verbal communication skills in English.

Required skills

• Regulatory submission preparation and dossier management.
• Lifecycle management of pharmaceutical products.
• Risk assessment and mitigation planning.

What we offer

• Opportunity to work with a global leader in healthcare innovation.
• Exposure to cross‑regional regulatory processes.
• Fixed‑term contract with potential for extension based on performance.