PROCESS VALIDATION INTERN

Description

Position Summary: You will provide support in process validation activities, documentation preparation, and coordination with support departments within the EPD division. Key Responsibilities: 1. Support in documentation and process validation activities. 2. Field tracking of validation batches. 3. Internal coordination with support departments. **About Abbott** Abbott is a global healthcare leader that creates 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 matters, grow and learn, take care of yourself and your family, be authentically you, 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 best place to work in dozens of countries worldwide and named one of the world's most admired companies by Fortune. * A company recognized as one of the best large workplaces, as well as a top workplace for diversity, working mothers, women executives, and women scientists. **The Opportunity** This position is located at the Lince headquarters in 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 Process Validation Intern, you will support the department in process validation activities, including documentation preparation (protocols, reports), field tracking of validation batches, and internal coordination with support departments (Quality Control, Technical Operations, Manufacturing, Quality Assurance). **What You'll Do?** * Support in documentation activities (protocols and reports). * Field tracking of validation batches. * Internal coordination with support departments (Quality Control, Technical Operations, Manufacturing, Quality Assurance). **Required Qualifications** * Graduate in Pharmacy and Biochemistry. * Preferably with experience in the pharmaceutical industry. * Intermediate-level English proficiency. * Intermediate-level Microsoft Office proficiency. * Preferably knowledgeable in quality tools. * Availability to work at the Lince Plant site. * Availability to work on-site Monday through Friday, from 8:30 AM to 6:00 PM. **Abbott is an equal opportunity employer and conducts recruitment, selection, and hiring based solely on job-related qualifications, without regard to race, color, religion, creed, age, sex, national origin, gender identity or expression, sexual orientation, disability, marital status, veteran or military status, or genetics.**