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Ajusta redacao dos curriculos

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ltadeu6 2026-04-06 19:33:02 -03:00
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8
curriculo-en.tex
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@ -14,18 +14,18 @@ ltadeu6@protonmail.com | linkedin.com/in/ltadeu6 | github.com/ltadeu6
\end{center}
\section*{Summary}
Bioprocess and Biotechnology Engineer with experience in finished product quality control in the pharmaceutical industry and team leadership. Strong background in data analysis, programming (Python), and scientific research, focused on applying computational tools to biotechnology and industrial processes.
Bioprocess and Biotechnology Engineer with experience in finished-product quality control in the pharmaceutical industry and team leadership. Strong background in data analysis, programming (Python), and scientific research, focused on applying computational tools to biotechnology and industrial processes.
\section*{Experience}
\textbf{Prati-Donaduzzi} \\
Quality Control Analyst \hfill 2023 -- Present \\
Quality Control Intern \hfill 2022 -- 2023
\begin{itemize}[noitemsep]
\item Perform assay (dosage) and impurity control in quality control routines
\item Operate 5 HPLCs (UV/Vis) and run about 10 analyses per day in pharmacopeial and local methods
\item Perform assay (dosage) and impurity testing in quality control routines
\item Operate 5 HPLCs (UV/Vis) and run about 10 analyses per day in pharmacopeial and locally developed methods
\item Coordinate a 2-4 person team preparing mobile phase and samples
\item Check documentation and lead the first step of deviation investigations (OOS/OOT) with reanalysis and counter-samples
\item Create automations in HPLC operations to speed up spreadsheet sharing
\item Create workflow automation in HPLC operations to speed up spreadsheet sharing
\item Work with dosage forms such as tablets, capsules, liquids, ointments, and emulsions
\item Ensure compliance with Brazilian Pharmacopeia, USP, and ANVISA audits
\item Use Empower and SAP for analysis workflows and records

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curriculo-ptbr.tex
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@ -22,11 +22,11 @@ Analista de Controle de Qualidade \hfill 2023 -- Atual \\
Estagiário -- Controle de Qualidade \hfill 2022 -- 2023
\begin{itemize}[noitemsep]
\item Realizar doseamento e controle de impurezas em rotina de controle de qualidade
\item Operar 5 HPLCs (UV/Vis) e conduzir cerca de 10 análises diárias em métodos farmacopeicos e locais
\item Coordenar equipe (2 a 4 pessoas) no preparo de fase móvel e amostras
\item Operar 5 HPLCs (UV/Vis) e conduzir cerca de 10 análises diárias em métodos farmacopeicos e de desenvolvimento local
\item Coordenar equipe (2 a 4 pessoas) no preparo de fase móvel e de amostras
\item Conferir documentação e conduzir a primeira etapa de desvios (OOS/OOT) com reanálises e contraprovas
\item Criar automatizações na operação de HPLCs para agilizar o compartilhamento de planilhas
\item Atuar com formas farmacêuticas como comprimidos, cápsulas, líquidos, pomadas e emulsões
\item Atuar com formas farmacêuticas de comprimidos, cápsulas, líquidos, pomadas e emulsões
\item Assegurar conformidade com Farmacopeia Brasileira, USP e auditorias da ANVISA
\item Utilizar Empower e SAP no fluxo de análises e registros
\end{itemize}