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Summary

Ho sempre nutrito un grandissimo interesse per le discipline scientifiche, in particolare per le scienze farmaceutiche. Infatti, dopo il diploma di maturità scientifica ho acquisito la Laurea Specialistica in Chimica e Tecnologie Farmaceutiche, successivamente, per ampliare le mie conoscenze e per comprendere le dinamiche legislative ed economiche globali del mercato Farmaceutico, ho acquisito il diploma di Master di II Livello in Discipline Regolatorie presso l’università di Pavia. Da Giugno 2015 lavoro come QC specialist presso l'Haupt Pharma Latina srl, proseguendo la carriera nel QC iniziata nel Gennaio 2013 presso la Janssen CCilag SpA, in più ho un 'esperienza di 7 mesi come Pharmacovigilance & Regulatory Affairs Internship at the Otsuka Pharmaceutical Italy s.r.l. SACRIFICO giornalmente alcune ore alla FORMAZIONE e al MIGLIORAMENTO CONTINUO perché voglio essere in grado di fornire il massimo contributo in termini di prestazioni lavorative oltre a volere soddisfare la mie curiosità e ambizioni "LA MIGLIORE PREPARAZIONE PER DOMANI E FARE DEL TUO MEGLIO OGGI"​(H. Jackson Brown) Negli anni di studio sono riuscito ad autofinanziarmi, grazie alle numerose borse di studio vinte durante la laurea specialistica, grazie anche alle mie doti sportive nonché al lavoro svolto presso lo studio fotografico di mio Padre In 17 anni di attività agonistica come calciatore dilettante,ho acquisito un'ottima propensione al lavoro di squadra, al raggiungimento degli obiettivi prefissati, al confronto costruttivo e al rispetto delle gerarchie. In fine grazie alle mie esperienze lavorative ho imparato a essere critico, collaborativo, pro-attivo preciso, affidabile, scrupoloso, puntuale e dedicato.

Experiences

Current Experience

  • QC Specialist
    Since July 2015
    • Safeguarding Quality of Products • Performing Analysis to the Raw Materials, API, finished products according to European Pharmacopoeia, US Pharmacopoeia, Japanese Pharmacopoeia, British Pharmacopoeia, Good Quality Control Laboratory Practice (GQCLP) also according to the Analytical Specifications • Supporting the Supervisor and the team either in the management of Out Of Trends, Out Of Specifications, Quality investigations (LIR), further in the management of deviations and CAPA • Writing and reviewing SOPs, Work Instructions, Sampling and testing procedures for APIs and raw materials. • Supporting in editing activities of Quality Specifications • Checking & reviewing raw-data for Raw materials and GMP critical documentations • Validating and implementing NIR library (Identification of Raw Materials) • Supporting QC department during several Inspections performed by Regulatory Authority (FDA, AIFA, MHRA....) and customers

Past Experience

  • quality control
    January 2013 --- June 2015
    • Safeguarding Quality of Products • Performing Analysis to the Raw Materials according to European Pharmacopoeia, US Pharmacopoeia, Japanese Pharmacopoeia, Good Quality Control Laboratory Practice (GQCLP) also according to the Analytical Specifications • Supporting the Supervisor and the team either in the management of Out Of Trends, Out Of Specifications, Quality investigations, further in the management of deviations and CAPA • Editing periodic reports of Environmental and Water Analysis • Writing and reviewing SOPs, Work Instructions, Sampling and testing procedures for APIs and raw materials. • Supporting in editing activities of Quality Specifications • Checking & reviewing raw-data for Raw materials and GMP critical documentations • Validating and implementing RAMAN library (Identification of Raw Materials) • Supporting QC and QA department during several Inspections performed by Regulatory Authority (FDA, AIFA, MHRA....) and customers

  • Pharmacovigilance & Regulatory Affairs Internship
    April 2012 --- October 2012
    • Supporting Pharmacovigilance & Regulatory Manager in editing and retention/archiving of all documentation concerning Pharmacovigilance activity and Regulatory Affairs activity • Managing and writing several deviation reports concerning Safety (Individual Case Safety Reports, Periodic Safety Updated Reports) and Quality of Pharmaceutical Products (Product Quality Complaint). • Monitoring Italian, European and extra European rules and laws about Pharmaceutical products • Supporting in writing and reviewing SOPs and Work Instructions • Reviewing and checking promotional or informational material and SmPC

  • Part-time Photographer and cameraman operator/assistant
    January 2001 --- January 2011

  • Intern chemist
    February 2009 --- July 2009
    Experience in public contact work and knowledge of proper ethical behavior, experience in reading the prescriptions and forwarding them, in reading pharmaceutical formulation, temperature and storage conditions, laws about narcotic and psychotropic substances, knowledge of administrative and technical organization of Chemist’s.

Personality

Self Assessment :
Attention to detailCollaborationCritical thinkingCuriosityEfficiencyCoordinationFlexibilityIndependenceInterest in knowledgeOrientationProblem solvingResiliencyStrategic thinkingResponsibility

Knowledge

LinkedIn Assessment :
Regulatory affairsSOPQuality ControlPharmaceutical IndustryQuality SystemPharmaceutical SciencesTeamworkchemical analisysAzioni correttive e preventiveGMPgas chromatographyLiquid chromatographyFTIRPharmacovigilanceBuona pratica di laboratorioComplianceClinical monitoringPhotographyDrug SafetyICSRsRaw MaterialsFDA GMPGMP JPGVPUS PharmacopoeiaJapanese PharmacopoeiaEuropean PharmacopoeiaAccurate Data EntryCross-team CollaborationTeam BuildingUV-Visatomic absorption spectroscopyLaser DiffractionUS FCC

Skills and Expertise

Self Assessment :
Assist with routine testsPerform routine testsAttend seminars, courses and meetings within and outside the companyout

Education

  • Master in Integrated Management Systems: Quality, Environment, Safety & Energy from ISTUM in 2016
  • Master in Pharmaceutical Regulatory Sciences from Università degli Studi di Pavia / University of Pavia in 2013
  • Degree in Chemistry and Pharmaceutical Tecnology from Università di Catania / University of Catania in 2011
  • High school leaving qualifications in from Secondary high school of Science “E. Medi” Leonforte in 2004

Training and Certification

  • Certificate of Professional qualifying: Chemist Certification
  • Lean Six Sigma Yellow Belt Certification

Languages

BrightOwl Assessment:
Self Assessment:
Italian
Native
English
Professional Proficiency

Work Preferences

  • Notice Period:
    3 weeks
  • Positions I am interested in:
    Associate Scientist Chemical Analyst GMP Coordinator Industrial Pharmacist Laboratory Assistant Lab Scientist QA Officer QA Consultant Regulatory Affairs Associate Regulatory Affairs Consultant
  • Locations I am interested in:
  • Work From Home:
    No
  • Work Regime:
    Permanent position
    BrightOwl employee
  • International:
    Yes

Area / Region

Latina, Province of Latina, Italy

Others

Driving License
  • Yes