Deivid Nogueira Rafael

Deivid Nogueira Rafael is a CQV Expert at PQE Group since January 2022, specializing in consulting for life science companies, particularly in the pharmaceutical sector, to ensure compliance with local and international regulations such as ANVISA, FDA, EU-GMP, and TGA. Prior experience includes roles in maintenance and validation engineering at Hosp-Pharma and Fresenius Kabi Brasil, where responsibilities encompassed contract and team management, project oversight for equipment acquisition, and adherence to validation protocols. Deivid has also held validation analyst and technologist positions at Novartis Brasil and Cristália Produtos Químicos Farmacêuticos Ltda, focusing on equipment qualification, quality management systems, and maintenance programs. Educational qualifications include an MBA from FGV with a focus on project management, a Master’s in health system administration from Uninove, and a Bachelor’s in electrical engineering from FESP, along with a technologist degree in industrial automation from IFSP.