About Abbott

Abbott is a global healthcare leader who is creating breakthrough science to improve people’s health. We always look towards the future, anticipating medical science and technology changes. We are dedicated to expanding access to our trusted medicines in some of the world's fastest-growing countries. Our extensive portfolio includes high-quality, differentiated branded generic medicines that cover various therapeutic areas, such as gastroenterology, women's health, cardiometabolic health, pain management/central nervous system disorders, and respiratory diseases.

Working at Abbott

At Abbott, you can do work that matters, grow and learn, care for yourself and your family, be your true self and live a whole life. You will have access to:

Career development with an international company where you can grow your dream career.A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies by Fortune.A company recognized as one of the best big companies to work for and the best place for diverse working mothers, female executives, and scientists.

The Opportunity:

Abbott is seeking an experienced Regional Regulatory Affairs Manager to lead regulatory strategy, market access, and pricing activities across a multi‑country cluster. This role works closely with regional teams, government authorities, and industry stakeholders to enable successful product launches, lifecycle management, and sustainable business growth.Key Responsibilities

Regulatory Strategy & Business Support

Define and implement short‑, medium‑, and long‑term regulatory strategies aligned with business objectivesProvide strategic regulatory guidance to internal teams, distributors, health authorities, and industry associationsLead product registrations, new indications, line extensions, renewals, and variationsMonitor healthcare policy, pricing, and reimbursement trends and develop effective response strategiesTranslate regulatory strategy into actionable plans while proactively managing risks and issues

Operational Excellence

Oversee country Regulatory Affairs teams across the clusterEnsure execution of regulatory activities including submissions, labeling, clinical trial support, licenses, and post‑marketing lifecycle managementPrepare and deliver regulatory plans that support sales, market share, and profitability goalsManage pricing strategies, reference pricing reviews, and authority submissions in collaboration with Finance

Market Intelligence & Business Development

Partner with Business Development and Marketing on product portfolio expansionProvide regulatory input across all stages of product development and lifecycle planningTrack market, competitor, and market‑access trends to identify risks and opportunitiesAnticipate regulatory obstacles and develop cross‑functional solutions

People Leadership

Lead and develop Regulatory Affairs teams in a matrixed, multicultural environmentDrive performance management, talent development, succession planning, and coachingFoster a high‑performance culture focused on collaboration, accountability, and growth

Business Partnering & External Engagement

Build and maintain strong relationships with Ministries of Health, payers, and key stakeholdersAct as area label coordinator, working closely with QA, manufacturing, and global teamsSupport value proposition development and partnership initiatives

Compliance & Quality

Ensure compliance with regulatory, quality, and corporate SOPsSupport continuous improvement initiatives and training complianceChampion Abbott’s values and ethical standardsKey Success FactorsStrong influencing, communication, and stakeholder‑management skillsDeep understanding of local regulatory and healthcare environmentsProven ability to translate strategy into execution and resultsCollaborative leadership style with a track record of building high‑performing teamsQualifications & ExperiencePharmacy degree requiredMinimum 5 years’ experience in Regulatory Affairs within the pharmaceutical industryExperience in multinational or regional roles preferredStrong knowledge of regulatory requirements across multiple countriesFluent in French and English (Arabic is an advantage)