* Quality Management key user in SAP implementation * April 2017 until May 2018. * Responsible for: * Cleaning, preparation, submission and validation of the QM data * Review of quality processes to meet SAP GBS requirements across all interface areas * Support Master Data Material (MDM) processes for material registration * Parameterization of quality rules for data migration. * Laboratory Analyst (microbiological and chemical-physical vaccines). * Responsible for: * Physical-chemical analyses (dosage of live vaccines by bacterial titration, pH, humidity, hemagglutination inhibition, purity) in live and inactivated vaccines * Development and validation of analytical methodologies for vaccine testing * Investigation of analytical deviations * Support change control to exchange specifications, suppliers or analytical methodologies * Equipment control: calibrations and validations, deviation investigations, negotiation with suppliers equipment and calibrations and maintenance services * Review analytical procedures and quality processes.

* Master Data Analyst * Material Master Data and XSteps Key user. * Responsible for: * Master recipe and bill of material creation and maintenance * Development and maintenance workflows to data collected with Excel interface * XSteps (PI sheets) maintenance and development * Support in the SKU's creation and maintenance, in the SAP system * End user training * Development and review the quality procedures related with the above activities * Participate of the investigations, change controls and CAPA's in the TrackWise tool * Support the project team for new product introduction, geographic extension, product characteristics and packaging changes * Strong relationship whit the production, planning and quality areas to ensure the data quality of all SKU's and Master Recipes in SAP.

* Laboratory Analyst (microbiological and chemical-physical vaccines).Responsible for:- Physical-chemical analyses (dosage of live vaccines by bacterial titration, pH, humidity, hemagglutination inhibition, purity) in live and inactivated vaccines * Development and validation of analytical methodologies for vaccine testing * Investigation of analytical deviations * Support change control to exchange specifications, suppliers or analytical methodologies * Equipment control: calibrations and validations, deviation investigations, negotiation with suppliers equipment and calibrations and maintenance services * Review analytical procedures and quality processes. Show less

* Responsible for: * Management of microbiological analyzes: raw material, finished product, stability, environmental, water, dosage of antibiotics, as well as management of a team of nine people * Request materials for laboratory routine * Analysis of non-compliance processes * Products release * Results reports * Participate of external and internal audits * Applicability of GLP standards * BPF and 5S.Experience in : SAP, Protheus and Sphere systems for analytical/laboratory management and people management. Show less

* Responsible for:Analytical results management the SAP System * Analytical Schedules * Physicochemical and microbiologics analysis, following current national and international legislation, of meat products in natura, industrialized, raw material, effluents and water * Reagent control via SAP system and excel spreadsheets * Maintenance of the 5S tool, and of Good Laboratory and Manufacturing Practices, as well as auditing in other sectors.Experience in adapting the analytical routines to the increase in the demand for analysis, with the same physical resources and people of the previous demand.Knowledge in national and international legislation for the adequacy of analyzes according to the requirements of each market.Experience in the PDCA tool to solve laboratory deviations. Show less

* Responsible for: * Physic-chemical analyzes (titration, UV/VIS spectrometer, infrared spectrometer, atomic absorption spectrometer, thin layer chromatography, Karl Fischer) in pharmaceutical raw materials; * Experience in the investigation of analytical deviations; * Ability to interpret pharmacopoeias, analytical methods and pharmaceutical legislation, applied to laboratory routine, as well as BPF, GLP and 5S.