Directing and supervising the project management office from Research and Development department, managing both departmental and project resources. Key activities and achievements include:• Implementation of processes and methodologies to optimize project execution.• Development and coordination of strategies to improve team communication and collaboration, resulting in increased efficiency and productivity.• Reduction of project execution times by 20% through the implementation of efficient management practices.• Implementation of project tracking systems and resource management tools to ensure optimal resource allocation and effective budget management.• Strengthening project management office operations to improve control of departmental and project resources.• Implementation of risk management processes and mitigation plans, considering financial impacts on projects.

Supervise and direct all company operations, including product development and manufacturing, logistics, procurement, quality management, project management, budgeting, and staff selection and training. Key responsibilities and achievements include:• Comprehensive management of laboratory operations, overseeing formulation development, product manufacturing, quality control, and regulatory compliance.• Implementation of improvements in formulation development processes, resulting in increased production efficiency.• Leadership in implementing quality management systems to ensure regulatory compliance and internal quality standards.• Successful supervision of new product line launches, from development to commercial production, meeting established deadlines and quality standards.

Facilitate the technology transfer of pharmaceutical formulations, ensuring a smooth and efficient transition to commercial production. Develop strategies to optimize manufacturing processes, thus improving the operational efficiency of the products under my responsibility.

Lead the implementation of the decommissioning plan and the closure for the R&D facilities from GSK Consumer Healthcare Mexico.• Successful decommissioning and closure of the R&D pilot plant, warehouse, and laboratory facilities from GSK Consumer Healthcare Mexico

Design, optimization and transfer of manufacturing procedures personal care products. Preparation of Standard Operating Procedures, and the registration documents to submit to the local health authority to obtain the authorization for cosmetic products.• Implementation of quality tools such as the Design of Experiments (DoE) for the quality by design (QbD) process for key projects under the responsibility of the technology transfer area to evaluate the impact of the processing parameters in the quality attributes.• Responsible for performing GEMBA analysis with an international multidisciplinary team for the simplification of the manufacturing process for one of the company's flagship products.• Implementation of the risk analysis tool (FMEA) during the technology transfer stage for key projects, integrating and managing project teams with relevant personnel.• Establishment of the technology transfer / Process Science area in Darier, in accordance with global guidelines from GSK.• Lead the qualification and implementation of GMP pilot plant and warehouse facilities, HVAC and processing equipment, and the cleaning validation strategy for pilot plant, warehouse, and equipment.• Establishment of academic interactions between GSK R&D and academic institutions in Mexico.

Design, optimization and transfer of formulas and manufacturing procedures for solid and semisolid pharmaceutical dosage forms. Preparation of Standard Operating Procedures, and the registration documents to submit to the local health authority to obtain the authorization for pharmaceutical and cosmetic products. Lead the product development projects from conceptualization to plant implementation.• Design, optimization, and transfer of the manufacturing processes of 12 formulas, obtaining reproducible results at different manufacturing scales.

Establishment of the oncology products division and implementation of working methodologies for the R&D area in the company.

Development of formulations and manufacturing processes for pharmaceutical products. Technology transfer of pharmaceutical solid dosage forms including cough drops, medicated jellies, syrups, and tablets. Compilation and preparation of CMC and R&D documentation for product registration.

Responsible for the development, manufacturing, and scaling of solid pharmaceutical forms, including the formulation of bilayer tablets and sustained-release products. Main activities included:• Preparation of protocols, development and stability reports, and CMC documentation for regulatory registration.• Contribution to the preparation of documents for product patents and for regulatory registration with health authorities of New Products.• Creation, programming, and validation of Excel spreadsheets with macros for formulation and other processes to optimize internal processes.