At **Corporativo DL**, we are seeking an **Analytical Development Manager** to lead and coordinate the development, validation, and transfer of analytical methods for the characterization and quality control of pharmaceutical products. This key role ensures compliance with national and international regulatory requirements, as well as the standards demanded by our clients and auditing agencies. ### **Main Responsibilities** * Lead the design, validation, and transfer of analytical methods for quality control and product release. * Coordinate the planning and execution of analytical studies related to development, technology transfer, and continuous improvement. * Supervise and validate technical documentation such as manufacturing orders, procedures, and stability studies, ensuring their accuracy and compliance. * Ensure analytical methods comply with regulatory guidelines and client requirements. * Effectively manage human, technical, and material resources within the department. * Coordinate calibration and maintenance of analytical equipment to ensure precision and operational readiness. * Promote continuous improvement strategies in analytical development and control processes. * Represent the department during internal and external audits, ensuring accurate documentation and regulatory compliance. * Provide specialized technical support to production, quality, and regulatory departments. ### **Profile Requirements** **Education:** * Degree in Chemical Engineering (professional title and license required). **Experience:** * Minimum 10 years in analytical development within the pharmaceutical industry. * At least 2 years in leadership or technical management roles. **Key Knowledge:** * Development and validation of analytical methods under ICH Q2 guidelines. * Inter-laboratory and plant-to-plant analytical method transfer. * Formulation and characterization of pharmaceutical products. * Good Laboratory Practices (GLP) and compliance with national and international regulations. * Technical leadership and project management. * Technical documentation and handling of regulatory audits. ### **We Offer** * Job stability in a company committed to quality and innovation. * Professional growth in a regulated and highly technical environment. * Additional benefits beyond legal requirements. * Continuous training and opportunities for advancement. * **Join Corporativo DL and contribute your expertise to the development of high-quality pharmaceutical products.**