A leading Pharmaceutical Laboratory is incorporating an Engineering Analyst to ensure the proper operation, continuous improvement, and reliability of plant equipment and facilities, guaranteeing compliance with GMP standards, safety, environmental regulations, and current regulations. Responsibilities Manage and execute engineering projects. Analyze failures and propose improvements to increase the reliability of critical equipment. Develop and update technical documentation (protocols, reports, drawings, manuals). Provide technical support to Production and Quality Control. Implement energy consumption optimization projects and new technologies. Ensure compliance with safety, hygiene, and environmental regulations. Monitor indicators (KPIs) and generate management reports. Requirements Industrial, Mechanical, Electronic, Chemical Engineer or related fields. 3 to 5 years of experience in engineering, maintenance, or projects within the pharmaceutical industry or similar under GMP regulations. Knowledge of GMP (ANMAT, FDA, EMA). Experience with critical systems (HVAC, water, gases, electricity). Project management (ideally PMO, MS Project or similar). Technical English. Competencies valued Analytical and problem-solving skills. Proactivity and results orientation. Teamwork and good communication. Organization and priority management. **Location:** Avellaneda **Modality:** 100% on-site – Full-time