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biotech and International Relations graduate, interested in the legal/regulatory framework concerning the Life Sciences, especially at eu level.

past experience in the eu commission and in private companies.

steadfast, committed, practical, proficient in English and French.

looking for positions concerning quality and/or regulation (qa/qc, ra, ip etc.).


Past Experience

  • Trainee Brussels, Belgium

    March 2016 --- July 2016

    vbb traineeship in the cabinet of commissioner for Health and Food Safety, vytenis andriukaitis

    assistance in the Policy making for the following issues:
    - Health technology assessment
    - new (plant) breeding techniques and synthetic Biology regulation
    - glyphosate re-authorization process, endocrine disruptors criteria setting

  • Validation Engineer Various

    January 2011 --- July 2012

    external Consultant for pharma/MD industry - quality and technical Validation

    - Risk Assessment, according to FMEA and HACCP techniques, applied to design and Manufacturing process of plastic components of Medical Devices;
    - enforcement of Change Control protocols concerning bloodlines for haemodialysis;
    - drafting and review of standard operative procedures (sops) in order to ensure GMP Compliance of internal activities;
    - drafting, review and implementation of Qualification/Validation protocols (iq/oq/pq)
    - review of internal records to verify their conformity to sops and gdp Compliance

  • Junior Researcher Naples, Italy

    March 2010 --- April 2010
    standard bio-Laboratory practices (blotting, cloning, Cell culturing etc.)


Self Assessment :
Attention to detailCollaborationCritical thinkingDiligenceKindnessOrganizationResiliencyProblem solvingStrategic thinkingCoordination


Self Assessment :
BiochemistryBiotechnologyGMPSOPQuality Assurance (QA)Quality Control (QC)
LinkedIn Assessment :
EU PoliciesEU LawQuality Assurance (QA)BiotecnologPolitical AnalysisEnglishFrenchInternational RelationsPolitical SciencePharma PolicyEudraLexExcelWordPowerPointMac OS XProcess ValidationTechnical DocumentationTechnical QualificationsQuality Control (QC)Regulatory affairsProduct ValidationHACCPFailure Mode and Effect Analysis (FMEA)AutoCADPhotoshop

Skills and Expertise

Self Assessment :
Create SOPsArchive documentation Develop protocols Write protocolsAdministrative supportAdvise on strategyAssist with proceduresConduct literature searchesCoordinationRegulatory documentationManage regulatory activitiesMaintain Quality Management System (QMS)Develop Quality Risk Management (QRM) initiatives


  • Laurea I Livello - Bachelor's Degree in Affari e relazioni internazionali from Università di Bologna in 2014
  • Erasmus in Biologia Molecolare from Université de Liège in 2009
  • Laurea I e II Livello - BSc + MSc in Biotecnologie Industriali from Università degli Studi di Napoli 'Federico II' in 2009
  • Maturità Classica in inglese, latino, biologia, greco, chimica from Liceo Ginnasio Statale "Pietro Colletta" - Avellino in 2004
  • Master in Euro-Progettazione 2014-2020 in from Europa Cube Innovation Business School in 0000

Training and Certification

  • Diplôme d'Études en Langue Française (DELF) in 0000 Certification
  • First Cerificate in English (FCE) in 0000 Certification


BrightOwl Assessment:
Self Assessment:
Professional Proficiency
Professional Proficiency

Work Preferences

  • Notice Period:
    2 weeks
  • Positions I am interested in:
    QA Officer Regulatory Affairs Officer Administrative Assistant GMP Operator Regulatory Affairs Assistant
  • Locations I am interested in:
    Austria Belgium Canada France Germany Italy Luxembourg Netherlands Sweden Switzerland United States
  • Work From Home:
  • Work Regime:
    Permanent position
    BrightOwl freelancer
    BrightOwl employee
  • International:

Area / Region

Aiello del Sabato, Province of Avellino, Italy


Driving License
  • Yes

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