Company: Lupin

Location: CMX, MX

Job Description Coordinate the planning and execution of validation/applicability, optimization, and transfer programs for analytical methodologies (pharmacopoeial and non-pharmacopoeial) for new developments, reformulations, and raw materials, both in internal and external national and international laboratories. Define strategies based on risk analysis, pharmacopoeias, standards, and literature. Review and approve protocols and reports, ensuring compliance with GLP, GDP, and GMP, as well as the proper execution by the personnel in charge. Manage material resources, equipment, and supplies, guaranteeing compliance with the area's programs. Participate in internal and external audits related to the area. Provide technical support to formulation, development, production, and quality. Manage special projects and urgent analytical validation requests. Prepare and update area documentation in accordance with GLP, GDP, and GMP. Ensure the p...