Refina headlines e impacto
This commit is contained in:
parent
9a368b6154
commit
0441640642
8 changed files with 73 additions and 66 deletions
|
|
@ -9,24 +9,25 @@
|
|||
|
||||
\begin{center}
|
||||
\textbf{\LARGE Lucas Tadeu Marculino} \\
|
||||
Engineer focused on quality control and regulatory compliance \\
|
||||
Toledo, PR, Brazil \\
|
||||
ltadeu6@protonmail.com | linkedin.com/in/ltadeu6 | github.com/ltadeu6
|
||||
\end{center}
|
||||
|
||||
\section*{Summary}
|
||||
Bioprocess and Biotechnology Engineer specialized in finished-product quality control, regulatory compliance, and deviation investigations. Hands-on experience with HPLC, OOS/OOT, and GMP/GLP standards.
|
||||
Bioprocess and Biotechnology Engineer specialized in finished-product quality control and deviation investigations, working in a GMP/GLP environment. Hands-on experience with HPLC, OOS/OOT, and regulatory compliance.
|
||||
|
||||
\section*{Experience}
|
||||
\textbf{Prati-Donaduzzi} \\
|
||||
Quality Control Analyst \hfill 2023 -- Present \\
|
||||
Quality Control Intern \hfill 2022 -- 2023
|
||||
\begin{itemize}[noitemsep]
|
||||
\item Operational scale: operate 5 HPLCs (UV/Vis) and process about 10 analyses per day for finished products
|
||||
\item Perform assay (dosage) and impurity testing ensuring accuracy and reliability of analytical results
|
||||
\item Lead deviation investigations (OOS/OOT) at the first stage with reanalysis and counter-samples after documentation checks
|
||||
\item Coordinate mobile phase and sample preparation with a 2-4 person team to keep throughput steady
|
||||
\item Ensure compliance with Brazilian Pharmacopeia, USP, and ANVISA audits
|
||||
\item Use Empower and SAP for traceability and critical quality records
|
||||
\item Operate 5 HPLCs (UV/Vis) and process about 10 analyses per day for finished products, ensuring result consistency
|
||||
\item Perform assay (dosage) and impurity testing with traceability, ensuring analytical reliability
|
||||
\item Lead deviation investigations (OOS/OOT) at the first stage with reanalysis and counter-samples, ensuring regulatory compliance
|
||||
\item Coordinate mobile phase and sample preparation with a 2-4 person team, maintaining workflow flow
|
||||
\item Ensure compliance with Brazilian Pharmacopeia, USP, and ANVISA audits, strengthening compliance
|
||||
\item Use Empower and SAP for critical quality records, ensuring traceability
|
||||
\end{itemize}
|
||||
|
||||
\section*{Education}
|
||||
|
|
@ -36,8 +37,8 @@ Quality Control Intern \hfill 2022 -- 2023
|
|||
|
||||
\section*{Research \& Projects}
|
||||
\begin{itemize}
|
||||
\item Capstone (TCC): built a computational tool (HTML, JavaScript) to optimize fermentation parameters
|
||||
\item Implemented bioleaching parameter optimization in Python with data analysis and modeling
|
||||
\item Capstone (TCC): built a computational tool (HTML, JavaScript) to optimize fermentation parameters, accelerating analysis
|
||||
\item Implemented bioleaching parameter optimization in Python with data analysis, supporting technical decisions
|
||||
\end{itemize}
|
||||
|
||||
\section*{Skills}
|
||||
|
|
|
|||
Loading…
Add table
Add a link
Reference in a new issue