• Product safety for Latin America market for baby diapers products.• Elaboration of safety assessments that support human health and chemical regulatory compliance of finished products, considering identified hazards and exposure according to the intended product use.• Preparation of risk assessment for raw materials and finished goods, supporting business needs from current production to innovation.• Review of supplier documentation.• Creation and control of records on SAP system to maintain material and product compositional and chemical compliance data.• Review of projects, claims strategies, post marketing surveillance and safety tests (humans and in vitro strategies).• Collaboration in cross-company projects.• Marketing claims discussion and substantiation. Rationale for tests in order to support marketing claims.• Collaboration and support cross-functional teams as R&D, Quality, Regulatory Affairs, Post-Marketing Surveillance, etc.• Project management.• Risk communication.• Strategic Thinking.• Consumer Product Safety.

Toxicological assessments and setting health-based exposure limits (HBEL) for active pharmaceutical ingredients; risk management process to control cross-contamination risks; literature review in scientific databases focusing on the evaluation of the toxicity of each active substance, considering preclinical and clinical data; critical analysis of toxicological studies focused on scientific robustness and data quality; preparation of HBEL Reports for APIs, based on EMA, ASTM, PIC/S, ICH, ISPE’s RiskMaPP and Anvisa guidelines; review of toxicological information for the identification of active substances presenting endpoints such as Genotoxicity, Carcinogenicity, Reproductive Toxicology, Developmental Toxicology and Highly Sensitizing, with the aim of assisting in decision- making on the priority of toxicological evaluation and establishment of the PDE and adequacy of cleaning validation; toxicological evaluation of new molecules. Extractables and leachables assessments. Occupational risk assessment. Read across assessment. REACH/ECHA, CLP, GHS and (Q)SAR knowledge.

- Responsible for the guidance, development and validation of analytical methods for drugs of abuse using chromatography and mass spectrometry techniques in hair samples (LC-MS/MS).- Optimization of routine methods for greater efficiency and lower cost, as well as fast resolution of analytical problems. - Technical skills in Waters, Thermo and Agilent instruments. - Certified Scientist according to CONTRAN No 691 DE 27/09/2017, NIT-DICLA-069, Feb/2019,03, ABNT NBR ISO/IEC 17025.- Supervision and release of results. - Team management.

Forensic toxicological analyses usingchromatographic and mass spectrometry techniques for detection of drugs of abuse in hair samples. Sample processing, release of reports, corrective maintenance of LC-MS/MS, LDTD- MS/MS and GC-MS/MS. Technical skills in Waters, Agilent and Sciex instruments.

Area: ToxicologyDetection of anabolic androgenic steroids and its biotransformation products in dried urinespots by paper spray-mass spectrometry ionization (PS-MS/MS)

Internship at the Analytical Toxicology Laboratory.

Internship in clinical analysis. Background in Abbott and Sysmex platforms.

Development of laboratory activities in Occupational Toxicology, analysis of urine and plasma samples by GC-MS and HPLC-MS. Validation of method for GC-FID. Development and validation of an analytical method for determination by atomic absorption in graphite furnace of plasma antimony concentration in the treatment of localized cutaneous leishmaniasis. Project carried out at the Faculty of Pharmacy of UFMG.

Institute of Criminalistics. Drug detection through colorimetric, chemical and toxicological tests. Use of GC-MS, LC-MS / MS, Thin Layer Chromatography and Infrared Spectroscopy.

Teaching assistant in Clinical Hematology.

Scenario analysis of the development of diagnostic and therapeutic products for Chagas' disease: from intellectual protection to commercial availability.