João Pilar is a biochemist and Master’s candidate in Biopharmaceutical Sciences with experience across pharmaceutical Quality Control, Quality Compliance, and Research & Development environments. He has worked in GMP-regulated laboratories performing analytical testing, stability studies, and documentation management in accordance with regulatory standards. His expertise includes HPLC and UPLC analysis of finished pharmaceutical products and stability samples, TLC analysis, and Karl Fischer titration, using platforms such as Agilent and Waters Alliance and Acquity. He has also contributed to SOP and stability protocol preparation, reagent and inventory management, and digital quality systems including LIMS and Veeva. In R&D settings, João has supported the development of oral solid dosage forms, working with tablet compression, powder blending, milling, and capsule filling. He has experience handling potent and non-potent compounds, operating in controlled humidity and temperature environments, and applying techniques such as NIR analysis and tablet characterization testing. João combines a strong scientific foundation with hands-on industry experience and a commitment to quality, precision, and continuous improvement within pharmaceutical development and manufacturing.…João Pilar is a biochemist and Master’s candidate in Biopharmaceutical Sciences with experience across pharmaceutical Quality Control, Quality Compliance, and Research & Development environments. He has worked in GMP-regulated laboratories performing analytical testing, stability studies, and documentation management in accordance with regulatory standards. His expertise includes HPLC and UPLC analysis of finished pharmaceutical products and stability samples, TLC analysis, and Karl Fischer titration, using platforms such as Agilent and Waters Alliance and Acquity. He has also contributed to SOP and stability protocol preparation, reagent and inventory management, and digital quality systems including LIMS and Veeva. In R&D settings, João has supported the development of oral solid dosage forms, working with tablet compression, powder blending, milling, and capsule filling. He has experience handling potent and non-potent compounds, operating in controlled humidity and temperature environments, and applying techniques such as NIR analysis and tablet characterization testing. João combines a strong scientific foundation with hands-on industry experience and a commitment to quality, precision, and continuous improvement within pharmaceutical development and manufacturing.WWWW…