Abbott is a global healthcare leader, driven by the mission of creating breakthrough science to improve people’s health. Recognized worldwide as a great place to work, Abbott operates in more than 160 countries with a focus on helping people live more fully at all stages of life. The company is frequently recognized by Fortune as one of the world’s most admired companies and stands out for its commitment to diversity, innovation, and development opportunities.

Position Overview
Abbott is seeking an experienced Regulatory Affairs & Quality Assurance Manager for its operations in Dubai, covering the Gulf, Egypt, Levant (GEM & LEVANT) regions. This is a full-time position with responsibilities spanning regulatory compliance, quality systems management, team leadership, and cross-functional coordination to ensure product and process excellence.

Key Responsibilities

Regulatory Affairs (GEM & LEVANT):

• Lead all regulatory activities including product registration, renewals, variations, labeling, site transfers, and pricing documentation.

• Prepare and submit regulatory dossiers aligned with country-specific requirements.

• Serve as the primary point of contact for health authorities, responding to queries and managing product lifecycle compliance.

• Coordinate internal reviews and align regulatory documentation with internal systems.

• Manage change controls, training compliance, archiving, and tracking of submissions and approvals.

• Provide regulatory input during tenders and ensure timely updates of local product lists.

• Supervise preparation and accuracy of SOPs and internal documentation related to regulatory functions.

Quality Assurance (GEM & LEVANT):

• Oversee quality systems and ensure compliance with internal and external regulations.

• Manage quarterly management reviews, internal audits, complaint handling, and CAPA processes.

• Supervise the quality manual, audit readiness, risk management, material control, and cold chain logistics.

• Lead initiatives related to geo-expansion and cybersecurity in compliance with global SOPs.

• Ensure robust supplier management and cross-departmental quality collaboration.

• Maintain training compliance and act as a trainer for local quality procedures.

Project Coordination:

• Define project requirements, timelines, and deliverables.

• Assign responsibilities, track progress, manage risks, and ensure timely execution.

• Support financial tracking including P&L statement preparation.

• Act as the communication bridge across stakeholders, project leads, and internal teams.

Required Qualifications

• Bachelor’s degree in a relevant field.

• 8–10 years of experience in regulatory and quality roles within the pharmaceutical industry.

• Strong understanding of local and regional health regulations.

• Demonstrated leadership and cross-functional coordination skills.

• Excellent communication, analytical, and problem-solving abilities.

Why Join Abbott?

• Career growth opportunities in a global company.

• Recognized as a top employer for diversity, working mothers, scientists, and female executives.

• Comprehensive support for professional and personal well-being.

To learn more about Abbott, visit www.abbott.com, follow us on Facebook at facebook.com/Abbott, or Twitter at @AbbottNews and @AbbottGlobal.