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Experiences

Current Experience

  • R&D Scientist


    Since September 2013
    Research Scientist- Pharmacokinetics and Toxicology • • responsible for In Vivo adme studies, as study Director. • use of high throughput Automation machines as: hamilton, tecan. • use of ab sciex api 4000, api 4000qt ms, waters aquity uplc, agilent 1100 HPLC with ctc pal • handling of different matrices (blood, plasma, urine, brain, lungs etc) • customers support, direct contact with clients, delivering results to clients. • duties include HPLC and uplc setup, mass spectrometer calibration and optimization, method development lc/ms/ms Analysis, chromatographic peak integration, providing assistance with method Troubleshooting, and performing Documentation, as appropriate • serves as mentor to newer/less experienced staff • attend kick off meeting Research Scientist- Pharmacokinetics and Toxicology • • Responsible for in vivo ADME studies, as Study Director. • Use of High Throughput automation machines as: Hamilton, Tecan. • Use of AB Sciex API 4000, API 4000QT MS, Waters Aquity UPLC, Agilent 1100 HPLC with CTC PAL • Handling of different matrices (Blood, Plasma, Urine, Brain, Lungs etc) • Customers support, direct contact with clients, delivering results to clients. • Duties include HPLC and UPLC setup, mass spectrometer calibration and optimization, method development LC/MS/MS analysis, chromatographic peak integration, providing assistance with method troubleshooting, and performing documentation, as appropriate • Serves as mentor to newer/less experienced staff • Attend kick off meeting

Past Experience

  • Scientist LC/MS/MS

    January 2013 --- July 2013
    responsible for the operation and maintenance of lc/ms equipment. duties include HPLC setup, mass spectrometer calibration and optimization, lc/ms/ms Analysis, chromatographic peak integration, providing assistance with method Troubleshooting, and performing Documentation, as appropriate attend kick off meetings serves as mentor to newer/less experienced staff preparation of HPLC solution following glp guidance.

  • Scientist 1 LCMS

    November 2011 --- January 2013
    responsible for the operation and maintenance of lc/ms equipment. duties include HPLC setup, mass spectrometer calibration and optimization, lc/ms/ms Analysis, chromatographic peak integration, providing assistance with method Troubleshooting, and performing Documentation, as appropriate attend kick off meetings serves as mentor to newer/less experienced staff preparation of HPLC solution following glp guidance.

  • LC/MS/MS Scientist I

    May 2010 --- November 2011
    responsible for the operation and maintenance of lc/ms equipment. duties include HPLC setup, mass spectrometer calibration and optimization, lc/ms/ms Analysis, chromatographic peak integration, providing assistance with method Troubleshooting, and performing Documentation, as appropriate preparation of HPLC solution following glp guidance.

  • Herbicide Formulation Chemist

    April 2006 --- May 2010
    Research and development to improve or make new Formulations for herbicides and seed treatments responsibilities include bench scale and scale-up Formulations including weighing, mixing, milling, air drying. interpretation, investigation and Analysis of new Formulation physical properties perform physical Testing on wet and dry formulated products provide Innovation, Leadership, Technical Support and guidance in issues related to product field complaints use of brookfield viscometer, UV, karl-fisher, tga q50 thermogravimetric analyzer, dsc q2000 differential scanning calorimeter, anton paar physica mcr 301 rheometer, kruss tensiometer, mastersizer 2000 particle size machine, eiger beads mill, bench top extruder and fluid bed dryer, bench top hammer mill, sturtevant micronizer.

  • QA Validation team

    April 2002 --- May 2004

  • Process Validator

    April 2002 --- April 2004
    responsibilities include preparing, writing, executing and reviewing of installation Qualification (iq), operation Qualification (oq), performance Qualification (pq) following the internal quality standards, current Good Manufacturing Practice (cGMP) and Good Laboratory Practice (glp) from 21 cfr 210 -211 participated with project teams, strong interaction with manufacturing, Quality Control and Chemistry labs participated in factory acceptance test (fat) and site acceptance test (sat) for new Pharmaceutical equipments analyze data, write and review of Validation reports, master batch record, Validation final reports developed standard operating procedures (sops) worked in class b and class c rooms for production batch Validation of oncologic drugs (liquid and /or freeze-dried) used laboratory information management system (LIMS) to report data results

  • Organic Chemist

    July 1999 --- December 2001
    group in the Medicinal Chemistry division synthesized and investigated the composition and molecular structures of new compounds including steroids, flavonoids, and benzopyranones, as potential antagonists of the aromatase Enzyme interpretation, Analysis and investigation of physical and chemical properties of new compounds used infra red spectrometry (ir) and nuclear magnetic resonance (NMR) to evaluate the new compounds

  • Chemist

    April 1999 --- June 1999
    organic Chemist in the dr. marco de amici group preparation of chiral enantiopure heterocyclic derivatives endowed with Biological activity used gas chromatography (gc) and high pressure Liquid chromatography (HPLC) for purity evaluation of the heterocyclic derivatives

  • Technical Manager

    February 1999 --- March 1999
    involved in technical direction and Quality Control

Personality

Self Assessment :
Analytical thinkingStrategic thinkingSelf-confidenceResponsibilityResult OrientedProblem solvingOptimismInterest in knowledgeCuriosityCreative thinkingCollaboration

Knowledge

Self Assessment :
Lab scale batches Labtechnician Negotiation R&D Scientific writingValidationTroubleshootingTrainingTechnical SupportTeam BuildingTeachingStudy protocolsStandard Operating Procedure (SOP)SpectroscopySmall moleculesscienceSamplingResearchProtocolProtein PurificationBioanalysisBioavailability
LinkedIn Assessment :
GLPMass SpectrometryBiotechnologyChemistryValidationcGMPChromatographygas chromatographyLIMSGMPFormulationLaboratoryHPLCLC-MSSOPNMROrganic ChemistryMedicinal ChemistrySOPHigh-Performance Liquid Chromatography (HPLC)Good Laboratory Practice (GLP)Pharmaceutical IndustryResearch and Development (R&D)Life SciencesDrug DiscoveryFormulazioneStandard Operating Procedure (SOP)

Skills and Expertise

Self Assessment :
Develop protocols Lab scale batches Report data

Education

  • Chimica e Tecnologie Farmaceutiche in from Università degli Studi di Milano in 1997
  • MS in Chemistry and Pharmaceutical Technology from State University of Milan in 1997
  • Master’s Degree in from U.S. equivalency in 0000

Languages

BrightOwl Assessment:
Self Assessment:
Italian
Native
English
Full Proficiency

Work Preferences

  • Notice Period:
    6 weeks
  • Work From Home:
    No
  • Work Regime:
    Permanent position
  • International:
    Yes

Area / Region

Verona, Province of Verona, Italy

Others

Driving License
  • Yes

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