Marina Farias Email & Phone Number

I am a passionate pharmacist, dedicated to ensuring the quality and safety of products in the pharmaceutical industry. With a master’s degree in Bioactive Natural and Synthetic Products (UFPB), and as I currently pursue a Ph.D. in Technological Development and Innovation (UFPB/USP), I maintain a solid academic background combined with extensive practical experience in quality assurance.As a Validation Specialist at Hemobrás on the Buriti Project, which aims to implement the national production sector for recombinant coagulation Factor VIII, I perform various essential activities to ensure the compliance of processes and products. I possess extensive experience and the necessary qualifications to work in the area of equipment and systems qualification within the pharmaceutical industry, ensuring compliance with Good Manufacturing Practices (GMP) and regulatory standards. I engage in the activation and execution of qualifications for equipment, utilities, and systems, ensuring high-quality production. My responsibilities include reviewing technical documentation, such as P&IDs and specifications for systems and utilities, as well as developing and reviewing qualification documents (DQ, IQ, OQ, PQ), traceability matrices, and critical parameter evaluations. I am also responsible for writing Risk Assessments to define qualification strategies and maintain the validated status of systems and equipment.Communication and adaptability are strengths that I use to foster mediation and collaboration in dynamic environments. These experiences and skills provide me with a solid foundation to contribute effectively to qualification and validation projects within the regulated environment of the pharmaceutical industry.Analista de Garantia da Qualidade Pl. com foco em Validação na Hemobrás, no Projeto Buriti, que tem como objetivo implementar o setor de produção nacional do Fator VIII de coagulação recombinante, executo diversas atividades essenciais para assegurar a conformidade dos processos e produtos. Atuo na revisão de documentação técnica, como P&IDs e especificações de sistemas e utilidades, além de desenvolver e revisar documentos de qualificação (DQ, IQ, OQ, PQ), matrizes de rastreamento e avaliações de parâmetros críticos, elaboração de Análise de Risco para definir estratégias de qualificação e manter o estado validado dos sistemas e equipamentos.Soft Skills: Comunicação eficaz, Liderança. Resolução de problemas. Organização. Adaptabilidade. Trabalho em equipe. Tomada de decisão