Position Summary: Present and implement the Validation System model to meet current regulatory and technical reference requirements, ensuring the deployment and compliance with the Pharmaceutical Quality System’s technical guidelines. Key Highlights: 1. Lead the implementation of pharmaceutical quality systems. 2. Ensure compliance with regulations regarding validation and qualification. 3. Contribute to the continuous improvement of pharmaceutical processes. **Position Objective** Present and implement the Validation System model at the PiSA Group site or plant, ensuring compliance with current regulatory and technical reference requirements. **Responsibilities and Activities** Implement the PiSA Group Pharmaceutical Quality System’s Technical Guidelines. Ensure the deployment of required technical guidelines and/or procedures within the Pharmaceutical Quality Management System. Provide technical advisory support to the site and/or plant during the implementation of the Pharmaceutical Quality Management System model. Ensure compliance with the deployed Pharmaceutical Quality Management System model at the site or plant. Experience in qualification of equipment for controlled environmental conditions. Qualification and validation processes for areas, utilities, equipment, and processes. Norm 059-SSA1-VV "Good Manufacturing Practices for Medicinal Products". Proficiency in recent versions of Microsoft Office Suite (Word, Excel, PowerPoint). English (desirable). Artificial Intelligence (desirable). Bachelor’s degree in Chemical Engineering or related fields. Employment Type: Full-time Salary: Starting from $1.00 per month Benefits: * Savings fund * Discounts and preferential pricing * Option for indefinite-term contract * Life insurance * Cafeteria service * Discounted cafeteria service * Grocery vouchers Work Location: On-site employment