Regulatory Affairs Coordinator Tunisia - Contractor

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries.

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

• Career development with an international company where you can grow the career you dream of.

• A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.

• A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.

In Abbott’s Established Pharmaceuticals Division (EPD)

We are committed to bringing trusted, high-quality branded generic medicines to millions of people around the world. Our Regulatory Affairs team plays a vital role in ensuring compliance, supporting product registrations, and enabling patients to access innovative healthcare solutions.

The Opportunity

Regulatory Affairs Coordinator

As a Regulatory Affairs Coordinator, you will support product registration and lifecycle management activities while ensuring compliance with local regulatory requirements. You will work cross-functionally with commercial, medical, quality, logistics, and global regulatory teams to drive successful product launches, renewals, and variations.

This role will support Tunisia, but based our Abbott Algeria office

What You’ll Work On

Prepare and submit regulatory dossiers for new product registrations, renewals, and variations.

Develop and implement regulatory plans aligned with business objectives.

Collaborate with global and local regulatory teams to support product lifecycle management.

Work closely with manufacturing, quality, development, marketing, medical, and logistics teams to ensure regulatory compliance and timely execution of activities.

Review and approve promotional materials in accordance with regulatory guidelines.

Liaise with local regulatory authorities and maintain effective external relationships.

Ensure compliance with regulatory and quality SOPs while identifying opportunities for process improvements.

Manage regulatory documentation, archiving, and submission tracking according to local and global requirements.

Support submissions related to promotional and non-promotional activities, symposiums, and congresses.

Contribute to training initiatives and promote Abbott’s values and compliance culture.

Qualifications

Bachelor’s degree in Pharmacy (Pharmacist qualification preferred).

Experience in Regulatory Affairs within the pharmaceutical industry is preferred.

Strong understanding of regulatory registration processes, product lifecycle management, and compliance requirements.

Excellent communication and stakeholder management skills.

Ability to collaborate effectively across cross-functional teams.

Strong organizational skills with attention to detail and document management.

Proficiency in managing multiple priorities and meeting regulatory deadlines.

Join Abbott and help bring quality healthcare products to patients while building a rewarding career with a global healthcare leader.