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Start for FreeGianluca Ricci
Quality Control Lead Expert @Merck Group
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WORK HISTORY
Quality Control Lead Expert @Merck Group
EDUCATION
Sapienza Università di Roma
Laurea breve, Chimica
ABOUT GIANLUCA RICCI
WORK EXPERIENCE Jul 21 - Today Analytical Operations and Quality Control Lab Manager Merck KGaA - Biotech Development Center - Corsier-sur-Vevey, Switzerland Management of an international team of 9 people (Lab. Tech, Senior Tech, Scientist) Participation as QC end User to a large part of the BDC projects for ramp-up (Digital Team, Robotics, GMP readiness) Management, as Business Owner, GLIMS implementation by definition of needs for QC scope Participation definition of main workflows for GMP/non-GMP activities (focus on Stability GMP and samples management) Participation in start-up of high-tech analytical laboratories Management of individual employee performances and development plan Jun 20- Jul 21 QC Chromatography Lab Manager (Legacy products)Merck KGaA - Guidonia, Italy Review and approval of analytical data of all chromatographic method (UPLC, HPLC, GC, MS) for Legacy products through LIMS software Management of weekly planning for team of 9 people (Lab. Tech, Senior Tech, Scientist) Administration of the laboratory priorities as release testing, stability testing and Lean Projects Management of individual operator performance Management of deviation, investigation, not valid test, CCP (TrackWise System) Management of Laboratory GMP documentation Ensure that the safety regulations and internal procedures are followed strictly. Ensure the proper preparation of GMP documentation (eg SOPs, Reports, Protocols, etc.)Feb 16 - Jun 20 QC-Electrophoresis and WET Chemistry Lab Manager (IMP product) Merck KGaA - Guidonia, Italy Review and approval of analytical data of all compendial method and electrophoretic methods (CE-SDS, cIEF, SDS PAGE, GEL IEF) Management of weekly planning (10 people: Tech, Senior tech, Scientists) Administration of the laboratory priorities Management of individual operators performance Management of deviation and not valid test (TrackWise System) Management of GMP documentation Ensure that the safety regulations and internal procedures are followed strictly. Ensure the proper preparation of GMP documentation (eg SOPs, Reports, Protocols, etc.)Apr 14 – Feb 16 Junior researcher – QC Analyst Merck KGaA - Guidonia, Italy Performing of compendial analytical methods Worksheet excel validations Updating SOP with new pharmacopoeia Backs up computerized analytics data Ensure the correct compilation of GMP documentation (notebook, logbook, etc.)Aug 12 – Mar 14 QC- Lab TechincianI.B.A Molecular (Policlinico Tor Vergata, Rome, Italy)
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