PMO Brazil Awards Judging Committee Member (Volunteer)

➠ Gestão de pessoas e de equipe.➠ Atuação como Gerente do Escritório de Projetos.

∙ NPI / NPD project management;∙ CAPEX project management;∙ Management of schedules, resources, scope, costs, people, quality, acquisitions, risks and Stakeholders;∙ High complexity project management, such as modifications to WFI systems and utilities;∙ Launching new products, and managing activities for new product launches and technology transfer;∙ Projects that will bring significant saving to factory (approximately 700 thousand BRL / year);∙ Agile project management… Show more ∙ NPI / NPD project management;∙ CAPEX project management;∙ Management of schedules, resources, scope, costs, people, quality, acquisitions, risks and Stakeholders;∙ High complexity project management, such as modifications to WFI systems and utilities;∙ Launching new products, and managing activities for new product launches and technology transfer;∙ Projects that will bring significant saving to factory (approximately 700 thousand BRL / year);∙ Agile project management methodology - Scrum; Show less

∙ LQAPM (Local Quality Assurance Project Manager) of the expansion and construction project of a new Nexgard plant with prospect of expanding production from 160 million tablets to 200 million tablets. ∙ Quality leader of the Phoenix project that will cost 19 million euros; ∙ Coordination of project teams and application of high complexity technical knowledge in the area of Good Manufacturing Practices and Projects in Pharmaceutical Industry. ∙ High complexity technical decision… Show more ∙ LQAPM (Local Quality Assurance Project Manager) of the expansion and construction project of a new Nexgard plant with prospect of expanding production from 160 million tablets to 200 million tablets. ∙ Quality leader of the Phoenix project that will cost 19 million euros; ∙ Coordination of project teams and application of high complexity technical knowledge in the area of Good Manufacturing Practices and Projects in Pharmaceutical Industry. ∙ High complexity technical decision making, due to the proportion of the projects in which I participate. ∙ Validation and Qualification of equipment, instruments, software and computer systems, process lines, utilities (HVAC, compressed air, water PW - WFI). Show less

∙ Developed improvements in the systematics of thermal qualifications through purchase of software and hardware that save time of qualification and validation in more than 70%.∙ Responsible for planning and execution of projects in the pharmaceutical industry.∙ Responsible for the elaboration of schedules and scope of projects through MS Project.∙ Responsible for the preparation of documents for qualification plans, test protocols, pending protocols, risk analysis, preparation of… Show more ∙ Developed improvements in the systematics of thermal qualifications through purchase of software and hardware that save time of qualification and validation in more than 70%.∙ Responsible for planning and execution of projects in the pharmaceutical industry.∙ Responsible for the elaboration of schedules and scope of projects through MS Project.∙ Responsible for the preparation of documents for qualification plans, test protocols, pending protocols, risk analysis, preparation of qualification reports and execution of Qualification of equipment and computerized systems meeting the 21CFR PART11 requirements for pharmaceutical processes;∙ Experience in thermal equipment qualification, heating stations for packaging lines and autoclaves;∙ Experience with qualification of systems and utilities such as: HVAC systems, drinking water, pharmaceutical use water (PW and WFI), compressed air, cooling towers among other systems required for drug manufacturing.∙ Participation of technical committee to evaluate security risks pertinent to the implementation of new projects.∙ Coordination of technical teams, management of qualification plans (IQ, OQ and PQ), technical specification of equipment, projects of implementation of industrial networks systems, controllers, packaging lines and components that comply with GMP (Good Manufacturing Practices) and Good Laboratory Practices (GLP).∙ Monitor and certify the quality of services provided by third parties and attest to the conformity of equipment / systems to internal specifications and specific standards;∙ Coordination and monitoring of services provided by internal collaborators.∙ Development and mapping of performance and KPI indicators for presentation to Stakeholders.∙ Application of process improvements, technologies and new projects.∙ Realization of FAT's and SAT's for the delivery of equipment in accordance with the project. Show less

∙ Responsible for physical tests of product characterization and systems developed by the PUR Development Laboratory and the Technical Service Unit;∙ Tests on polyurethane foams such as core density, compression, permanent deformation, dimensional stability, traction, adhesion among others. ∙ Development of new formulations.∙ Administrative routines referring to recording results in databases and crossing information with previous tests.∙ Control of samples and waste to be… Show more ∙ Responsible for physical tests of product characterization and systems developed by the PUR Development Laboratory and the Technical Service Unit;∙ Tests on polyurethane foams such as core density, compression, permanent deformation, dimensional stability, traction, adhesion among others. ∙ Development of new formulations.∙ Administrative routines referring to recording results in databases and crossing information with previous tests.∙ Control of samples and waste to be incinerated.∙ Participated in training on behavioral management and emotional control. Show less

∙ Prepare and deliver training for Field Engineers.∙ Repair, installation, maintenance and qualification of equipment such as HPLC, LC / MS, GC, GC / MS, Atomic and UV Absorption among others.∙ Visits to customers and calls. Ministrar Familiarization with equipment and systems such as LC / MS and GC / MS. OpenLAB Chemstation and Ezchrom courses.∙ Validation and Qualification of Equipment and computerized laboratory systems.

∙ Support internal customer (sales, technical assistance, bidding and management) and external customer (customers, external vendors, external technical support and management). ∙ Provide advice in the area of laboratory and process instrumentation (application, installation), translation of catalogs, manuals and descriptive. ∙ Technical specifications of equipment. ∙ Repair of electrochemical and electronic equipment. ∙ Participation in publicity fairs. ∙ Research and development… Show more ∙ Support internal customer (sales, technical assistance, bidding and management) and external customer (customers, external vendors, external technical support and management). ∙ Provide advice in the area of laboratory and process instrumentation (application, installation), translation of catalogs, manuals and descriptive. ∙ Technical specifications of equipment. ∙ Repair of electrochemical and electronic equipment. ∙ Participation in publicity fairs. ∙ Research and development of analytical methods and new applications. ∙ External visits, to publicize the line and provide technical support. ∙ Translation of meetings, support to customers and suppliers abroad (Germany and USA). Show less

∙ Analysis and testing of electronic equipment for process control and laboratory analytical equipment; ∙ Equipment that controls process variables such as temperature, pH, conductivity, equipment for agriculture (flow control of nutrient dosage, soil control among others). ∙ Research and development of analytical methods, analysis and development of methods by automatic titration, analysis and development of methods by selective ions, instrumentation in general; ∙ Experience in… Show more ∙ Analysis and testing of electronic equipment for process control and laboratory analytical equipment; ∙ Equipment that controls process variables such as temperature, pH, conductivity, equipment for agriculture (flow control of nutrient dosage, soil control among others). ∙ Research and development of analytical methods, analysis and development of methods by automatic titration, analysis and development of methods by selective ions, instrumentation in general; ∙ Experience in technical assistance of analytical instrumentation; ∙ Organization and sealing of newly tested equipment. ∙ Experience with colorimetric analysis, ORP meters and process dissolved oxygen monitors; ∙ Process Controller Testing. ∙ Support and customer service; after-sales experience. Show less