Regulatory Affairs Algeria & EFA

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 objectives
• Provide strategic regulatory guidance to internal teams, distributors, health authorities, and industry associations
• Lead product registrations, new indications, line extensions, renewals, and variations
• Monitor healthcare policy, pricing, and reimbursement trends and develop effective response strategies
• Translate regulatory strategy into actionable plans while proactively managing risks and issues

Operational Excellence

• Oversee country Regulatory Affairs teams across the cluster
• Ensure execution of regulatory activities including submissions, labeling, clinical trial support, licenses, and post‑marketing lifecycle management
• Prepare and deliver regulatory plans that support sales, market share, and profitability goals
• Manage 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 expansion
• Provide regulatory input across all stages of product development and lifecycle planning
• Track market, competitor, and market‑access trends to identify risks and opportunities
• Anticipate regulatory obstacles and develop cross‑functional solutions

People Leadership

• Lead and develop Regulatory Affairs teams in a matrixed, multicultural environment
• Drive performance management, talent development, succession planning, and coaching
• Foster 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 stakeholders
• Act as area label coordinator, working closely with QA, manufacturing, and global teams
• Support value proposition development and partnership initiatives

Compliance & Quality

• Ensure compliance with regulatory, quality, and corporate SOPs
• Support continuous improvement initiatives and training compliance
• Champion Abbott’s values and ethical standards

Key Success Factors

• Strong influencing, communication, and stakeholder‑management skills
• Deep understanding of local regulatory and healthcare environments
• Proven ability to translate strategy into execution and results
• Collaborative leadership style with a track record of building high‑performing teams

Qualifications & Experience

• Pharmacy degree required
• Minimum 5 years’ experience in Regulatory Affairs within the pharmaceutical industry
• Experience in multinational or regional roles preferred
• Strong knowledge of regulatory requirements across multiple countries
• Fluent in French and English (Arabic is an advantage)