Senior Specialist Pharmacovigilance (Affiliate Safety Representative)

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 providing high-quality, trusted medicines that improve health outcomes and enhance lives around the world. Our teams work collaboratively to ensure patients have access to safe, effective, and affordable treatments while maintaining the highest standards of quality and compliance.

Abbott is seeking a highly motivated   Senior Specialist Pharmacovigilance (Affiliate Safety Representative)   to join our team in Tunisia. This role is responsible for ensuring that all pharmacovigilance activities for Abbott's registered and investigational medicinal products are conducted in compliance with local regulatory requirements and Abbott's global standards. As the local Pharmacovigilance representative, you will serve as the primary point of contact for health authorities, internal stakeholders, and global PV teams, helping to maintain a robust and compliant local safety system.

Act as the local Affiliate Safety Representative (ASR) and Local Safety Responsible (LSR). Maintain local pharmacovigilance procedures, documentation, and compliance requirements. Ensure timely receipt, recording, reconciliation, and reporting of safety information. Conduct   safety surveillance   activities, including literature and health authority website monitoring. Prepare and support local periodic safety reports and   Risk Management   Plans. Manage   regulatory submissions   related to pharmacovigilance activities. Deliver   pharmacovigilance training   to local employees and stakeholders. Maintain local PV product lists, records, and archives. Support vigilance requirements for medicinal products, medical devices, and food supplements. Coordinate and support pharmacovigilance audits, inspections, and compliance activities. Manage local PV agreements with distributors, partners, and service providers. Collaborate with internal and external stakeholders to ensure effective   safety reporting   and compliance. Support regional and global pharmacovigilance projects as required.

Required Qualifications Bachelor's degree in Pharmacy, Life Sciences, Medicine, or a related discipline. Strong understanding of pharmacovigilance principles and local regulatory requirements. Excellent communication and   stakeholder management   skills. Strong attention to detail and organizational abilities. Proficiency in   Microsoft Office   applications. Good command of English, both written and spoken.

A minimum of 4 years pharmacovigilance experience within the pharmaceutical industry ideally having worked within a multinational organization Experience supporting local regulatory authority interactions. Knowledge of   safety surveillance ,   case processing , and pharmacovigilance compliance activities. Why Join Abbott? At Abbott, you'll be part of a global healthcare leader committed to improving lives through innovative healthcare solutions. You'll have the opportunity to