Global Regulatory & Quality Assurance Leader

Abbott; Dubai; On-site; AED 300,000 - 550,000; Full time

Job summary

Abbott seeks an experienced Regulatory Affairs & Quality Assurance Manager in the United Arab Emirates. The role drives regulatory submissions, dossier preparation, and lifecycle management across GEM & LEVANT regions, ensuring compliance with local regulations.

You will coordinate cross-functional teams, review promotional materials for compliance, and maintain QA systems, documentation, and archiving to support timely product availability.

Qualifications

• Bachelor's degree required with 8–10 years in a similar pharmaceutical regulatory role.
• Experience with GEM & LEVANT regulatory processes and health authority interactions.
• Ability to review promotional materials according to Abbott policies and HA regulations.

Responsibilities

• Provide regulatory support across tender and market registrations.
• Prepare submission dossiers per country requirements and ensure timely renewals and variations.
• Coordinate country-specific regulatory activities and communicate with health authorities.
• Review and approve promotional materials per Abbott procedures and HA regulations.
• Maintain local product lists, SOPs, and archiving to ensure compliance and traceability.
• Lead project coordination with stakeholders to define scope, timeline and deliverables.

Skills

Regulatory affairs

Quality assurance

Project coordination

GMP/Regulatory compliance

Documentation management

Education

Bachelor's degree

Job description

Abbott seeks an experienced Regulatory Affairs & Quality Assurance Manager in the United Arab Emirates. The role drives regulatory submissions, dossier preparation, and lifecycle management across GEM & LEVANT regions, ensuring compliance with local regulations.

You will coordinate cross-functional teams, review promotional materials for compliance, and maintain QA systems, documentation, and archiving to support timely product availability.