Regulatory Affairs Senior Specialist – METAP & CIS

About the role

Abbott is seeking a Regulatory Affairs Senior Specialist to join its Established Pharmaceuticals division in the UAE. The role focuses on METAP and CIS products, supporting regulatory activities across multiple countries for a fixed‑term, one‑year assignment.

Key responsibilities

• Manage regulatory activities such as renewal registrations, variations, safety updates, pricing, labeling, and site transfers for assigned markets.
• Prepare and submit dossiers in accordance with country‑specific regulations.
• Respond to health authority queries and coordinate appropriate responses.
• Provide regulatory guidance to internal teams and external partners.
• Lead or support strategic regulatory initiatives and act as the regulatory representative on project teams.
• Engage with health authorities and support external engagement activities.

Required profile

• Bachelor’s degree in Pharmacy.
• 3‑5 years of experience in Regulatory Affairs within the pharmaceutical sector.
• Knowledge of registration requirements and strong analytical mindset.
• Fluent in Arabic and English.

Required skills

What we offer

• Career development within a global healthcare leader.
• Opportunity to work on diverse regulatory projects in a fast‑growing market.
• Inclusive workplace recognized for diversity and employee well‑being.