**Global Medical Safety Expert- Biosimilars** **About Abbott** Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology. **Working at Abbott** 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. **The Opportunity** This position works out of our Bogota in the Established Pharmaceuticals division. We are committed to bringing the benefits of our trusted medicines to more people in the world’s fastest-growing countries. Our broad portfolio of high-quality and differentiated branded generic medicines reaches across multiple therapeutic areas including gastroenterology, women's health, cardiometabolic, pain management/central nervous system, and respiratory As the Global Medical Safety Expert- Biosimilars you’ll to provide guidance, direction and expertise for pharmacovigilance activities within one`s responsibility. Leadership of Product Safety teams. Responsibility and accountability for the safety of all assigned EPD products to ensure compliance. **What You’ll Do** • Serves as a SPOC for Biosimilars in LATAM • Represents Abbott towards governmental agencies and other competent authorities related to Pharmacovigilance topics • Develops strategic risk management plans for assigned products • Reviews clinical study protocols, their reports and publications • Proactively understands regulatory framework, trends & requirements related to products and clinical studies • Provides safety expertise throughout all stages of global drug development • Develops and reviews safety information as part of reports submitted to regulatory authorities • Is accountable for the safety monitoring strategy (including ICSR, aggregate data and literature review) and reference safety information documents throughout a product’s lifecycle, thereby minimizing patient and product risk. • Performs Medical assessment during processing of solicited cases **Required Qualifications** + Doctor of Medicine (MD) + Experience with Biosimilars **Preferred Qualifications** + Minimum 3-5 years industry experience in Pharmacovigilance, Medical Affairs of Clinical Development + Fluent in English + Broad and proficient understanding and experience in Pharmacovigilance in the pharmaceutical industry or academia or equivalent + Experienced professional operating within the international arena or working across functional areas. Apply Now (https://www.jobs.abbott/) Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at www.abbott.com , on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal. An Equal Opportunity Employer Abbot welcomes and encourages diversity in our workforce. We provide reasonable accommodation to qualified individuals with disabilities. To request accommodation, please call 224-667-4913 or email corpjat@abbott.com