Validation Analyst

Description

Position Summary: A leading pharmaceutical laboratory is seeking a Validation Analyst to execute and support the qualification and validation of processes, equipment, and instruments, ensuring compliance with regulatory requirements. Key Highlights: 1. Professional development in the pharmaceutical sector. 2. Participation in key validation and qualification processes. 3. Contribution to quality and reliability standards. Validation Analyst – Pharmaceutical Laboratory A leading pharmaceutical laboratory requires a Validation Analyst for its team, who will be responsible for executing and supporting activities related to the qualification and validation of processes, equipment, instruments, and systems, ensuring compliance with established protocols, internal procedures, Good Manufacturing Practices (GMP), and applicable regulations for the pharmaceutical sector. We are seeking an organized, analytical, detail-oriented individual with the ability to manage technical documentation and collaborate effectively across various departments of the company. Key Responsibilities * Execute and support validation and qualification activities in accordance with established protocols and schedules. * Fulfill assigned responsibilities within validation processes, ensuring proper execution and documentation of activities. * Participate in activities related to calibration and qualification of instruments, equipment, and systems—either directly or as technical support. * Carry out required sampling, data collection, and analysis during validation studies, considering established priorities. * Collect, review, and organize information and evidence generated during validation and qualification activities. * Prepare supporting documents, reports, and technical documentation related to the department’s activities. * Update and maintain current procedures, work instructions, forms, and other documents under their responsibility. * Define, review, and control the documentation required for process execution in accordance with current procedures. * Ensure appropriate handling and use of assigned equipment, instruments, materials, and other resources necessary for performing their duties. * Identify and promptly report deviations, non-compliances, or situations that may affect validation activity outcomes. * Comply with the Quality Policy, GMP, internal procedures, and other company-established policies. * Support follow-up and closure activities arising from validation and qualification processes. Requirements * Degree in Pharmaceutical Chemistry, Chemistry, Chemical Engineering, Pharmaceutical Engineering, or related fields. * Experience in validation and/or qualification within the pharmaceutical industry. * Knowledge of Good Manufacturing Practices (GMP). * Knowledge of process, cleaning, system, equipment, and/or method validation, according to the scope of the position. * Proficiency in technical documentation and quality management systems. * Desired knowledge of equipment and instrument qualification, calibration, and management of validation protocols and reports. Competencies * Analytical ability. * Attention to detail. * Organization and planning. * Critical thinking. * Teamwork. * Effective communication. * Document management. * Compliance orientation. * Responsibility and commitment. Working Conditions Position: Validation Analyst Contract Type: Indefinite-term Salary: 2\.500\.000 Work Schedule: Full-time Work Location: Bogota, Northern Zone Why Work With Us? You will have the opportunity to advance professionally in the pharmaceutical sector, directly participating in validation and qualification processes that contribute to meeting quality standards and ensuring organizational process reliability. If you meet the profile and wish to join our team, apply now! Work Location: On-site employment