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Work Background
MSN LaboratoriesProject Manager & Alliance Brazil
Apr. 2021 - May. 2025São Paulo, Brazil• Spearheaded the launch of MSN Laboratories' subsidiary in Brazil, ensuring compliance with local regulations. • Developed a state-of-the-art quality control laboratory, enhancing product reliability and safety. • Collaborated with regulatory affairs to submit dossiers to ANVISA, facilitating successful market entry. • Coordinated pharmaceutical equivalence studies, reinforcing the integrity of our product offerings.
• Collaborate with key partneship with local companies.
Cipla Brasil LtdaProject Coordinator/Technical Responsible
Nov. 2016 - Mar. 2021Vargem Grande Paulista, Sao Paulo, Brasil• Spearheaded the implementation of a quality control laboratory, ensuring compliance with GLP and regulatory standards. • Coordinated regulatory affairs operations, including MA transfers and GMP applications, enhancing operational efficiency. • Managed pharmacovigilance responsibilities, contributing to improved safety and compliance metrics.
LUPIN LIMITEDMarket Intelligence Analyst
Mar. 2016 - Sep. 2016São Paulo Area, Brazil• Conducted comprehensive market analysis utilizing IMS HEALTH and CLOSE-UP data to identify trends and opportunities. • Evaluated performance indicators and market behavior to support strategic decision-making processes. • Assisted in the implementation of the Business Intelligence Department, enhancing portfolio analysis and market strategies. • Developed expertise in Microsoft Power BI through the DAT207x course, improving data visualization and reporting capabilities.
LUPIN LIMITEDPharmacist Responsible
Jul. 2013 - Mar. 2016Cotia• Spearheaded the quality control laboratory building project for Lupin in Brazil, ensuring compliance with health authority regulations. • Coordinated HVAC project implementation and layout design for the facility, optimizing operational efficiency. • Successfully negotiated and secured contracts for Lupin's São Paulo headquarters, overseeing a 500m² office layout development.
EMSRegulatory affair Supervisor
Jan. 2012 - Jun. 2013Hortolandia - SP• Supervised the registration process for new drugs, generics, and brand generics, ensuring compliance with ANVISA regulations. • Compiled and revised comprehensive dossiers for submission, facilitating timely approvals and market entry. • Collaborated with cross-functional teams to streamline regulatory processes, enhancing operational efficiency.
RBZ Marketing e Serviços Ltda.Quality Assurance of new/renewal register of IPA, Generic ans Similar Medicines.
Oct. 2010 - Mar. 2012Responsible for improving the quality of the technical pharmaceutical department:
- adequacy and updating projects;
- checklist product development; - analysis of scientific technical documetations of active pharmaceutical insume (DMF), raw material, new drugs registrations(Generic,Similars, Post registrer), evaluation of stability studies, method of validation and Dossier preparation according to ANVISA requirements.
Updating of existing ANVISA requeriments like: RDC nº899 of 2003, RDC nº57 of 2009 e IN 15 2009, RE 310 of 1 de setembro de 2004…
Technical support for Brazilian protocol documentations.
FMVZMaster Degree Student
Jan. 2009 - Jan. 2009São Paulo Area, Brazil
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