Description: We are seeking a Senior Researcher to work in Hortolândia, in an on-site model. . \#LI\-RM1 Responsibilities and duties: * Will work in the post-registration area of pharmaceutical products, supporting reformulation studies, process improvements, and regulatory adjustments, ensuring compliance with guidelines from national and international regulatory agencies. . * Will also resolve technical issues related to drug manufacturing and quality control, including responsibility for investigating deviations, identifying root causes, and proposing effective solutions, ensuring regulatory compliance and production efficiency. . * Collaborates with multidisciplinary teams to optimize processes and ensure excellence in pharmaceutical products. . Requirements and qualifications: * Knowledge of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP). . * Familiarity with national and international regulations (ANVISA, ICH, EMA, FDA). . * Knowledge of registration, post-registration, development, and manufacturing of pharmaceutical products. . * Hands-on experience with processes such as granulation, compression, and coating. . * Data analysis and statistical tools (Minitab or Excel). . * Understanding of bioavailability and bioequivalence concepts. . * Root cause analysis and CAPA implementation. . * Desirable: Proficiency in Windows, Office Suite, SAP, Power BI, Artificial Intelligence, and Six Sigma certification. . Additional information: * Health insurance. * Dental insurance. * Meal allowance. * On-site meals. ]]\> 2512210202551681364