Regulatory Affairs Manager – Algeria

About the role

Cipla is seeking a Regulatory Affairs Manager to lead all regulatory activities for the Algeria market. Reporting to the Regulatory Affairs Executive/Director, you will oversee new product submissions, registrations, variations and lifecycle management to ensure timely approvals and market access.

Key responsibilities

• Provide regulatory intelligence to senior management and the CEO to support strategic decisions.
• Lead dossier preparation, submission and follow‑up with Algerian health authorities and, where relevant, other North African jurisdictions.
• Guide Regulatory Affairs pharmacists and managers on pre‑ and post‑registration activities, ensuring compliance with internal protocols and external regulations.
• Coordinate with Integrated Product Development and external partners to gather required data and documentation.
• Develop and maintain stakeholder relationships across functions to secure necessary support for regulatory submissions.

Required profile

• Proven experience in regulatory affairs within the pharmaceutical or healthcare sector, preferably covering Algeria or North Africa.
• Strong understanding of local and international regulatory frameworks and submission processes.
• Excellent communication and stakeholder‑management skills.
• Ability to work autonomously while aligning with cross‑functional teams.

Required skills

• Regulatory dossier preparation and lifecycle management.
• Regulatory intelligence gathering and analysis.
• Knowledge of Algerian health authority requirements.