**Job Objective:** Responsible for planning, coordinating, and supervising equipment, facility, process, and system validation activities within the pharmaceutical plant, ensuring compliance with regulatory requirements (GMP, FDA, EMA) and the company’s quality standards. **Key Responsibilities:** * Develop, review, and approve validation protocols and reports (IQ, OQ, PQ) for equipment, processes, and critical systems. * Coordinate execution of manufacturing and cleaning process validation studies, ensuring reproducibility and regulatory compliance. * Supervise validation personnel, assigning tasks and monitoring adherence to schedules. * Ensure that changes to processes, equipment, or systems are fully validated prior to implementation. * Collaborate with Production, Quality, and Maintenance departments to ensure GMP-compliant operations. * Participate in internal and external audits, providing evidence of compliance and tracking corrective actions. * Maintain up-to-date validation documentation in accordance with current regulations. **Requirements:** * Bachelor’s degree in Chemistry, Pharmacy, Biochemistry, Chemical Engineering, or related field. * Minimum of 2 years’ experience in validation within the pharmaceutical industry. * Solid knowledge of GMP, ISO standards, and local and international regulations (FDA, EMA). * Experience in process validation, cleaning validation, HVAC, purified water, and critical systems validation. * Leadership, organizational, and effective communication skills. * Ability to plan, prioritize, and meet strict project deadlines. If you possess a meticulous approach and a passion for excellence in validation, we invite you to join our team. DL Corporate offers a dynamic work environment and an opportunity to make a significant contribution to the success of our Validation Department.