Regulatory Affairs Associate (1‑Year Fixed‑Term)

About the role

The Regulatory Affairs Associate will support product approval, maintenance and lifecycle activities for Takeda in Algeria. Working closely with cross‑functional teams, health authorities and external partners, the associate ensures regulatory processes are executed efficiently and in compliance with local and global regulations.

Key responsibilities

• Prepare and review application components, meeting materials and attend regulatory agency meetings.
• Evaluate local business and regulatory registration requirements for investigational and marketed products; produce assessment reports.
• Obtain Ministry of Health (MOH) approvals for promotional and non‑promotional materials.
• Ensure labeling compliance and timely submission of safety updates and reports.
• Maintain secure archiving of regulatory and technical documents.
• Keep local product information up‑to‑date in regional databases.
• Develop effective relationships with business partners, service providers and the local regulatory community.
• Support regional and international RA teams on specific projects.

Required profile

• Pharmacy graduate.
• Knowledge of Algerian regulatory requirements.
• At least 1 year of experience in regulatory affairs or a related pharmaceutical role.
• Strong attention to detail and ability to work in a fast‑paced environment.
• Excellent communication and negotiation skills.

Required skills

What we offer

• Fixed‑term contract (1 year) with a leading global pharmaceutical company.
• Opportunities to work directly with health authorities and gain hands‑on regulatory experience.
• Collaboration with regional and international regulatory teams.