**About Abbott** Abbott is a global leader in healthcare, creating innovative science to improve people's health. We are always looking ahead, anticipating changes in medical science and technology. **Working at Abbott** At Abbott, you can do meaningful work, grow and learn, take care of yourself and your family, be truly who you are, and live a full life. You will have access to: **The Opportunity** This position is located at the Lince headquarters within the EPD (established pharmaceutical products) division. Our broad portfolio of high-quality, differentiated-brand generic medicines spans multiple therapeutic areas, including gastroenterology, women’s health, cardiometabolic, pain management / central nervous system, and respiratory. As a Regulatory Affairs Coordinator, you will be responsible for developing and implementing innovative regulatory strategies and execution plans to expand the portfolio through obtaining sanitary registrations. **What You'll Do?** * Evaluate, prepare, submit, and follow up on technical dossiers for products to obtain the corresponding Sanitary Registration (New Product), as well as manage renewal processes and variations to keep product documentation updated. * Establish timelines for submission and/or approval of new registrations, variations, and renewals. * Participate in the development of regulatory strategies for new registrations, renewals, and variations to ensure continuity of product commercialization in the market. * Keep various company regulatory platforms updated. * Review and approve promotional materials under responsibility. * Collaborate with project teams and communicate progress to the Regulatory Affairs Manager. * Coordinate interactions with other departments to ensure compliance with regulatory requirements for daily operations. * Stay informed about any changes in legislation. Ensure labels comply with all applicable regulations. * Comply with LATAM regulatory remediation plans by providing required information from dossier supplier sites and submitting updates from CAPA plans per product according to defined deadlines. * Review and approve promotional materials under responsibility. **Required Qualifications:** * Academic Background: Degree in Pharmaceutical Chemistry * Minimum 4 years of experience in the pharmaceutical industry in Regulatory Affairs and/or Quality Control, or similar roles within the pharmaceutical industry * Knowledge of GMP. * Availability to work in Lince from 8:30 am to 6 pm **Abbott is an equal opportunity employer and conducts its recruitment, selection, and hiring based solely on job-related qualifications, without regard to race, color, religion, creed, age, sex, nationality, gender identity or expression, sexual orientation, disability, marital status, veteran or military status, genetics, or citizenship status, or any other condition protected by law.**