Regulatory Affairs Specialist

About the role

The Regulatory Affairs Specialist will manage all regulatory activities for Tunisia and Algeria within the New Africa region. Based in Algeria on a 12‑month contract, the role supports product registrations, variations, renewals and ensures compliance with local authorities.

Key responsibilities

• Manage registrations, variations and renewals for Tunisia and Algeria in line with local regulations and launch plans.
• Prepare, submit and follow up dossiers to obtain approvals from health authorities.
• Liaise with distributors, regulatory agents and authorities, handling queries and submissions.
• Maintain regulatory affairs systems, databases and trackers, ensuring data accuracy and timely updates.
• Coordinate artwork layouts, product information reviews and ensure promotional materials align with the approved SPC.
• Support pharmacovigilance activities in collaboration with the IMETA PV Manager and technical teams.

Required profile

• Bachelor’s degree in Veterinary Medicine or Life Sciences.
• Minimum 2 years of experience in Regulatory Affairs (human or animal health).
• Fluency in English, French and Arabic.
• Strong planning, organization and coordination abilities.
• Result‑oriented mindset with solid analytical and problem‑solving skills.

Required skills

• Regulatory dossier preparation and submission.
• Regulatory database management.
• Artwork and promotional material review.