Victor Caixeta Email and Phone Number
Victor Caixeta personal email
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rofessional with an MBA in Industrial Management, Bachelor's degree in Chemical Engineering, and approximately 10 years of experience in Regulatory Affairs. Experience in national and multinational companies of all sizes, in sectors such as Food, Sauces and Condiments, Preserves, Apicultural Products, Food Supplements, Medications (Injectables, Solids, Semi-solids, and Liquids), and Cosmetics.Expertise in regulation, compliance, analysis of raw materials, formulas, and finished products, as well as reviewing documentation for registration, renewal, or post-registration processes with ANVISA and MAPA, ensuring process compliance and excellence in all operations.Consolidated regulatory experience in innovative products, compliance, and food product exportation. Skilled in updating procedures and creating and implementing new work instructions as needed.Strong experience in regulatory analysis of formulas, creation of labeling statements, promotional materials, and advertising in accordance with current legislation.Keywords: Regulatory Affairs, Engineering, Food Safety, Food Product Development, Regulation, Food Labeling, Food Supplements, ANVISA, MAPA, Ministry of Agriculture, Health Registration, SIF, Good Manufacturing Practices, Work Instructions, Management Reports, Indicators.
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Gerente De Assuntos RegulatóriosPharmanectarState Of Minas Gerais, Brazil
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Regulatory Affairs CoordinatorKraft Heinz Company Sep 2023 - PresentGoias, Brazil- Regulatory coordination related to New Registration processes and Portfolio Maintenance of the company;- Direct involvement in the labeling processes of the Heinz, Hemmer, and Quero brands, belonging to Kraft Heinz;- Responsible for Regulatory implementation in Innovation Projects;- Analysis of Raw Material Specs (Technical Data Sheet, Nutritional, GMO, RTIQ, PIC, Contaminants, Microbiological, Pesticides, Migration, and Foreign Matter);- Analysis of product formulations for regulatory compliance according to current laws;- Analysis of Finished Product and its respective labeling;- Support to Commercial, Marketing, R&D, FSQ, and other teams;- Lead and coordinate regulatory compliance activities ensuring the company's products meet all applicable standards and regulations;- Development of operational flows between sectors to develop and implement regulatory compliance policies and procedures;- Knowledge and daily experience with the Agile Management model. -
Regulatory Affairs Specialist AnalystPharmanectar Group Mar 2020 - Aug 2023Belo Horizonte City- Founder of the Regulatory Affairs department in the company;- Manager responsible for the Regulatory Affairs department;- Presentations, planning, and regular alignments with the company’s presidency;- Team management, new projects, and portfolio maintenance;- Company registration with ANVISA for Food Supplements;- Company registration with the FDA;- Company registration with MFDS (South Korea);- Company registration with Single Window (China);- Approval of the industrial expansion project by the Ministry of Agriculture (MAPA) - Brazil;- Preparation of dossiers for new product registration processes, registration renewals, post-registration changes, and compliance with requirements;- Direct involvement with the PGA_SigSif system (products for human consumption);- Monitoring of MAPA and DIPOA legislation for products intended for human consumption;- Active participation in maintaining company compliance with RIISPOA regulations, Good Manufacturing Practices (GMP), and Hazard Analysis and Critical Control Points (HACCP).
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Technical Documentation Analyst - Drug Master File (Dmf)Hypofarma Dec 2019 - Mar 2020Ribeirão Das Neves City- Analysis of Drug Master File (DMF) – in compliance with global quality standards (ICH, EMA, FDA, and Brazil's ANVISA) in CTD format;- Analysis of the synthesis routes of raw materials, reports, and certificates related to Elemental Impurities, Residual Solvents, and Analytical Validations;- Comparative analysis between the documentation submitted in the registration vs. the previous version received vs. the current version, to evaluate potential post-registration changes and their impact on the company;- Maintenance of the company's DMF documentation – List of current documents, their respective manufacturers, versions, and status.
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Regulatory Affairs AnalystHypofarma Apr 2018 - Dec 2019Ribeirão Das Neves City- Preparation of Drug Dossiers, product renewal processes, post-registration inclusions and notifications of medications, new product registrations, and compliance with requirements;- Notification of Product Change Histories (HMPs), integrated into the Company's Technical Evaluation Opinion flow (PATE);- Monitoring and follow-up of change control along with the appropriate regulatory actions;- Follow-up on Public Consultations (CPs), Webinars, and ANVISA's Collegiate Board of Directors (Dicol);- Analysis of technical documentation from raw material suppliers (Drug Master File - DMF);- Analysis of documentation from all areas of the company, such as analytical validations, reports, production orders, etc.;- Review of packaging layouts and preparation of legal texts for medications (leaflets).
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Project ManagerTm1 - Retail & Live Mkt Jan 2015 - Mar 2016Nova Lima City- Negotiation with clients and suppliers through transparent relationships;- Planning, execution of the established scope, and continuous monitoring of all project stages and the team;- Focus on meeting established goals, deadlines, and costs, ensuring the quality of deliveries and team development;- Risk mapping to identify and plan mitigation strategies and their respective impacts.
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Engineering TechnicianSnc Lavalin - Minerconsult Dec 2008 - Aug 2013Belo Horizonte City- Conception and analysis of projects through the study of reports and probing tests;- Development of Process Routes and Utility Systems (from raw materials to refined products), sizing of equipment used in the routes, and preparation of mass and energy balances, always considering the approved CAPEX for the project;- Development of engineering flowcharts integrated with (instrumentation, electrical, mechanical, and civil) sectors;- Planning and preparation of Technical Evaluations, Process Descriptions, data sheets, equipment lists, calculation memories, flowcharts, block diagrams, among others.
Victor Caixeta Skills
Victor Caixeta Education Details
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Gestão Industrial -
Reconhecimento Portaria Mec 303 De 27/12/2012 (Dou 31/12/2102) -
Colégio CotemigInformática Gerencial
Frequently Asked Questions about Victor Caixeta
What company does Victor Caixeta work for?
Victor Caixeta works for Pharmanectar
What is Victor Caixeta's role at the current company?
Victor Caixeta's current role is Gerente de assuntos regulatórios.
What is Victor Caixeta's email address?
Victor Caixeta's email address is vi****@****ail.com
What schools did Victor Caixeta attend?
Victor Caixeta attended Fundação Getulio Vargas / Fgv, Centro Universitário Una, Colégio Cotemig.
What are some of Victor Caixeta's interests?
Victor Caixeta has interest in Social Services, Economic Empowerment, Politics, Education, Environment, Science And Technology, Arts And Culture.
What skills is Victor Caixeta known for?
Victor Caixeta has skills like Microsoft Project, Planejamento De Projetos, Autocad, Microsoft Office, Engenharia, Sistemas Operacionais, Microsoft Excel, Engenharia De Projetos, Planejamento, Processo, Engenharia De Processos, Projetos.
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Victor Caixeta Albuquerque
Federal District, Brazil
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