Samuele Cozzi is an Investigation & Process Improvement Specialist with 11 years of experience in the pharmaceutical sector and a master's in Pharmaceutical Chemistry and Quality Assurance. He has progressed from QC System Owner roles to leading deviation, root-cause and CAPA management for sterile product manufacturing at GSK, combining hands-on lab QA with systems-level process improvement. Certified Lean Six Sigma Black Belt and ISO 9001 Lead Auditor, he has driven DMAIC projects on assembly waste and glass delamination reduction, translating statistical methods into measurable production gains. His background in CSV, IOQ/TQ and data integrity gives him a rare blend of IT-controlled system validation and shop-floor troubleshooting. Fluent in English and learning Chinese, he pairs continuous learning and international curiosity with practical mentorship and audit readiness. Colleagues note his ability to turn inspection findings into governance and KPI frameworks that sustainably reduce recurrent deviations.
11 years of coding experience
3 years of employment as a software developer
Experimental Thesis, Medicinal and Pharmaceutical Chemistry, 105/110, Experimental Thesis, Medicinal and Pharmaceutical Chemistry, 105/110 at Università degli Studi di Firenze
Lean Six Sigma Green Belt Certification, Lean Six Sigma Green Belt Certification at CROSSNOVA
Auditor, Lead Auditor UNI EN ISO 9001:2015, Auditor, Lead Auditor UNI EN ISO 9001:2015 at UNIONE PROFESSIONISTI
Master in Pharmaceutical Quality Assurance, Master in Pharmaceutical Quality Assurance at m-Squared Consulting
High School Diploma, 80/100, High School Diploma, 80/100 at liceo scientifico Agnoletti
Contributions:15 pushes, 1 branch, 2 issues in 5 years 3 months
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Samuele Cozzi - Investigation & Process Improvement Specialist