Job Description**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 science and medical technology. **Working at Abbott** At Abbott, you can do work that matters, 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: * Professional development with an international company where you can build 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 by Fortune. * A company recognized as one of the best large workplaces, as well as a great place to work for diversity, working mothers, female executives, and scientists. **The Opportunity** This position is located at the Lince plant As a **Production Supervisor**, you will be responsible for supervising the quality of manufacturing solid, liquid, and semi-solid pharmaceutical forms, ensuring compliance with Good Manufacturing Practices and current Occupational Health and Safety regulations throughout all stages of the production process. **What You’ll Do:** * Supervise compliance with Standard Operating Procedures (SOPs) applicable to the area. Keep operation and equipment cleaning instructions up to date. * Supervise compliance with the manufacturing auxiliary medium (MAF HALB) in the established sequence. Maintain these documents updated. * Ensure data integrity in area records during manufacturing processes. * Verify, when applicable, power adjustment calculations. * Verify, when applicable, product splitting at the end of the manufacturing process. * Verify documentation for weighing controlled materials and inactivation of controlled materials. * Supervise environmental monitoring and control in manufacturing and storage areas. Control storage time for intermediates and bulk products. * Supervise cleaning and sanitization of facilities and/or equipment in the area, ensuring areas are clean and orderly. * Verify calibration of area instruments. * Verify execution of preventive and/or corrective maintenance of facilities, equipment, and instruments in the area. Generate corresponding corrective maintenance requests. * Report and timely close non-conformities, deviations, and change controls generated in the area, as well as follow-up on derived actions. * Promptly report unsafe acts and conditions, incidents, and accidents, and follow up on timely closure of resulting actions. * Supervise compliance with the monthly production schedule and coordinate timely with involved departments. * Propose and implement improvement ideas identified in the area in coordination with staff and relevant departments. * Coordinate with other departments activities related to their processes. * Conduct personnel selection for the area, process replacements, leaves, permits, vacations, and conduct performance evaluations for direct reports. * Verify staff participation in scheduled activities and maintain a positive work environment. * Provide initial and periodic training for direct reports according to job requirements. * Perform qualification and backup training for personnel in the area. **Preferred Qualifications** * Degree in Pharmaceutical Chemistry. * Experience in manufacturing processes for solid, liquid, and/or semi-solid pharmaceutical forms. * Minimum of one year of experience in production within the pharmaceutical industry. * Intermediate level English skills desirable. * Knowledge of audits. * Knowledge of non-conformities. * Availability to work in Lince. Pursue your professional aspirations with Abbott to gain 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 workforce diversity. Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott, and on Twitter @AbbottNews and @AbbottGlobal. as directed by your reporting manager.