**TECHNICAL SERVICES ANALYST** **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 work that makes an impact, grow and learn, take care of yourself and your family, be truly who you are, and live a fulfilling life. You will have access to: * Professional development with an international company where you can achieve 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 magazine. * A company recognized as one of the best large workplaces for working mothers, female executives, and scientists, and where diversity is valued. **The Opportunity** This position is located in Cali within the Established Pharmaceutical Products division. We are committed to bringing the benefits of our reliable medicines to more people in the world's fastest-growing countries. Our broad portfolio of high-quality branded generic medicines covers multiple therapeutic areas, including gastroenterology, women's health, cardiometabolic, pain management / central nervous system, and respiratory. **What You'll Do** * Responsible for managing technical activities related to maintenance services, * Verification and validation of laboratory equipment, instruments, and computerized systems, ensuring their proper functioning and reliability. * Will also participate in system setup, data backup, Audit Trail review, and technical support together with external providers, complying with quality management system guidelines and qualification, calibration, and validation processes. **Required Qualifications** * Professional in Chemistry, Pharmaceutical Chemistry, Engineering, or related fields * Experience in handling laboratory equipment and specialized software, as well as skills in teamwork, technical analysis, and process documentation. **Preferred Qualifications** * 1 to 3 years of experience * Training and knowledge in computerized system validation, metrology, and quality regulations (ISO, GMP, etc.),