Francesco Troiano Email and Phone Number
Francesco Troiano work email
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Francesco Troiano personal email
Important experience 10+ in QUALITY CONTROL area (SPECIALIST/ANALYST and LABORATORY) in pharmaceutical and biopharma company.Extensive experience on API products with fermentation upstream and chemical/purification downstreamMember of several project teams especially in startup faseGood knowledge of AIFA, EMA and FDA inspections.Experience as SITE MANAGER of a clinical production site (30/35) employees,Wide experience on API products plasma-derived produced in classified enviroments. Experience on site revamping, equipment qualification and maintenanceExperience in Quality Global Operations, Tech/Quality Customer Service and Auting to CMOs.Excellent relationship skills and team working .Good knowledge in problem solving and flexibility.Qualified Person.
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Qa Manager And Qp And Technical Customer Service ResponsibleChemi SpaMilan, It -
Qu Manager/Qp & Technical Customer Service ResponsibleChemi Spa Feb 2020 - PresentCinisello Balsamo, Lombardy, It- Quality Unit Manager and QP in an AIFA/EMA and FDA approved API Site, - Responsible of Technical Customer Service for Chemi SpA (API company manufacturer)- Italfarmaco CMOs quality support and management, audit performing/inspection readiness, quality support for specific project like regulatory dossier updating, regulatory authority inspection preparation
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Qualified PersonFresenius Kabi Apr 2019 - Sep 2019Bad Homburg, Hessen, DeBatch Release, Site Reference Person for AIFA and foreign customers, support Business Unit Regulatory Affair, Member for both Site Management and Site Quality meetings, Member of Business Unit monthly Quality meeting. Site Trainer for GEMBA Walks Company Project. -
Global Compliance SpecialistKedrion Biopharma Feb 2018 - Feb 2019ItIssuing and reviewing of Global Policies and Procedures, Support for technology transfers for QC, Global Change Control coordination on TrackWise system, (ex: management of Global documentation, suppliers management, implementation and update of Global CSV systems etc.). Involved directly in the Global Quality KPI project aimed to the creation on a data trend to use for the implementation of dedicated CAPAs. -
Site ManagerKedrion Biopharma Jan 2014 - Jan 2018ItSite's Strategic Plan approval, issuing and monitoring of Budget CAPEX - OPEX, (via SAP) and Head CountCoordination of: Production, Quality Control, Maintenance and General Services, Engineering (out source)As Site Responsible, participation to development projects where others Company Sites were involved.Site referent point towards: Procurement, Global HR, Global R & D, Legal Office, Global Operations.
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Quality Control SpecialistGnosis S.P.A. Dec 2009 - Dec 2013Performing of GMP analysis on Raw Materials, Finished Products, Critical Intermediates and Packaging Material. Development and validation of analytical methods, backup to the QC Laboratory Manager and IPC Lab supervisor. Drafting and revision of documentation such as SOP, protocols and reports, instrumental logbooks, analytical documentation
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Quality Control SpecialistPfizer Pharmaceuticals Sep 2005 - Dec 2009New York, New York, UsPerforming of GMP analysis on Raw Materials, Finished Products, Critical Intermediates and Packaging Material. Development and validation of analytical methods, backup to the QC Laboratory Manager and IPC Lab supervisor. Drafting and revision of documentation such as SOP, protocols and reports, instrumental logbooks, analytical documentation, verification of analyzes performed using both internal and EP-USP methods. Involved as member of Site Inspection Team in the preparation and participation to AIFA, EMA and FDA inspections. -
Quality Control Analyst/SpecalistBiosearch Manufacturing Oct 2002 - Sep 2005Performing of GMP analysis on Raw Materials, Finished Products, Critical Intermediates and Packaging Material. Development and validation of analytical methods, backup to the QC Laboratory Manager and IPC Lab supervisor. Drafting and revision of documentation such as SOP, protocols and reports, instrumental logbooks, analytical documentation, verification of analyzes performed using both internal and EP-USP methods. Involved as member of Site Inspection Team in the preparation and participation to AIFA, EMA and FDA inspections.
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Quality Control Analist/SpecialistBiosearch Manufacturing Apr 2004 - Oct 2004Implementing a Quality Control Laboratory in the new Pharmaceutical Plant startup phase
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Industrial Chemical DepartementBiosearch Manufacturing May 2002 - Sep 2002Training project in the Laboratory of Chemical Development, development of extraction, purification and modification of active fermentation broth on a pilot plant. In particular application of techniques of micro-and nanofiltration, chromatography, crystallization
Francesco Troiano Skills
Francesco Troiano Education Details
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University Of BasilicataChemistry -
Itis MateraChemical Technichan
Frequently Asked Questions about Francesco Troiano
What company does Francesco Troiano work for?
Francesco Troiano works for Chemi Spa
What is Francesco Troiano's role at the current company?
Francesco Troiano's current role is QA Manager and QP and Technical Customer Service Responsible.
What is Francesco Troiano's email address?
Francesco Troiano's email address is fr****@****zer.com
What schools did Francesco Troiano attend?
Francesco Troiano attended University Of Basilicata, Itis Matera.
What skills is Francesco Troiano known for?
Francesco Troiano has skills like Gmp, Validation, Hplc, Quality System, Fda, Analytical Chemistry, Quality Assurance, Pharmaceutical Industry, Chromatography, Quality Control, Uv/vis, Laboratory.
Who are Francesco Troiano's colleagues?
Francesco Troiano's colleagues are Lusi Alessandro, Gaetano De Gennaro, Giuseppe De Gaetano, Andrea Distaso, Samuele Ciceri, Camilla Sartori, Gianmarco Polce.
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