Chiara Pellegrini

QC Associate at Advaxia Biologics
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Contact Information
us****@****om
(386) 825-5501
Location
Greater Rome Metropolitan Area, IT
Languages
  • English -
  • Italian -

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Credentials

  • INTRODUCTION TO GOOD CLINICAL LABORATORY PRACTICE
    The Global Health Network
    Apr, 2023
    - Nov, 2024
  • Investigator Oversight
    TransCelerate BioPharma Inc.
    Jul, 2021
    - Nov, 2024
  • ICH GOOD CLINICAL PRACTISE E6 (GCP)
    The Global Health Network
    Jun, 2021
    - Nov, 2024
  • Qualifying examination for biologist section A
    Università degli Studi dell'Aquila
    Sep, 2020
    - Nov, 2024
  • Training to work in medium risk lab
    Istituto Superiore di Sanità
    Oct, 2019
    - Nov, 2024
  • Security lab
    Università degli studi Roma TRE
    Apr, 2019
    - Nov, 2024

Experience

  • Advaxia Biologics
    • Italy
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • QC Associate
      • Jan 2022 - Present

      Quality Control activities: - Release of clinical lots of recombinant adenovirus vaccine and stability studies by regulatory requirements EMA, FDA, AIFA - Test and inspection of products (including cell-based assays, Western Blot and Visual Inspection assays) - Maintenance of stable Mammalian cell cultures (HEK293T, Procell92 and HeLa) - Control of the manufacturing microbiological environments - Report and interpret results of scientific experiments for the preparation and timely delivery of drug substance (DS) or drug products (DP) - R&D project - Write, review and update SOP - GMP Compliance Show less

  • PQE Group
    • Italy
    • Business Consulting and Services
    • 700 & Above Employee
    • Laboratory Excellence Support Consultant
      • Nov 2021 - Jan 2022

      - Quality Assurance activities such as validation and GMP compliance - Collaborate with different computerized systems validation projects (CSV) in the pharmaceutical field - especially laboratory projects. - Review, manage and archive documents - Develop a validation plan GMP-based and work together with different stakeholders. - Quality Assurance activities such as validation and GMP compliance - Collaborate with different computerized systems validation projects (CSV) in the pharmaceutical field - especially laboratory projects. - Review, manage and archive documents - Develop a validation plan GMP-based and work together with different stakeholders.

  • London School of Hygiene and Tropical Medicine, U. of London
    • United Kingdom
    • Higher Education
    • 700 & Above Employee
    • Research Assistant
      • Feb 2021 - Aug 2021

      Research activity in the Department of Infection Biology within the Faculty of Infectious and Tropical Diseases- Conduct research into developing a highly specific and sensitive serological assayfor COVID-19- Construction of SARS-CoV-2 Virus-Like Particles (VLP) by mammalian expression system -Maintenance of stable Mammalian cell cultures (HEK293T and HeLa) and transfection of these- Purification VLP by sucrose gradient -Experience in performing microbiological contamination analyzes (e.g. sedimentation plates, contact plates and fingerprints)- Manage the whole documentation and data integrity Show less

    • Scientific Officer
      • Sep 2020 - Feb 2021

      Research activity and managerial support in the Department of Infection Biology- Development and analysis of a SARS-CoV-2 recombinant protein by the Baculovirus expression system- Establishment and maintenance of stable insect cell cultures (Sf9 and Tini Cells) and infection of these.- Experience as Junior Laboratory Manager: management of laboratory spaces, supervision of storage organization and supply of materials- Perform standardized protocols and procedures (like as cell-based assays, Western Blot and PCR) Show less

  • Istituto Superiore di Sanità
    • Research
    • 700 & Above Employee
    • Internship Trainee
      • Mar 2019 - Mar 2020

      Research activity in the Department of Food Safety, Nutrition and Veterinary Public Health - Construction of vectors, transformation and expression of recombinant proteins in microorganism strains - Establishment and maintenance of stable mammalian cell cultures (HEK293T) and experience with transfections (PEI, Lipofectamine) - Purification and analysis of recombinant proteins - Perform a variety of microbiological tests by SOPs and GLP (e.g. PCR, Affinity chromatography, SDS-PAGE, Western blotting, ELISA and Plaque-Assay) Show less

  • Università degli studi Roma TRE
    • Italy
    • Education Administration Programs
    • 700 & Above Employee
    • Internship Trainee
      • Oct 2018 - Dec 2018

      Worked in the Biotechnology Lab of Microorganisms - Generate plasmid preps and characterize by restriction enzime digests - Performing PCR, Gel electrophoresis and DNA, RNA or protein extraction from biological samples - Produce antibiotic stock Worked in the Biotechnology Lab of Microorganisms - Generate plasmid preps and characterize by restriction enzime digests - Performing PCR, Gel electrophoresis and DNA, RNA or protein extraction from biological samples - Produce antibiotic stock

Education

  • ALMA LABORIS Business School
    Executive Master in Marketing and Management Pharmaceutical Industry
    2021 - 2022
  • Università degli studi Roma TRE
    Master of Science - MS, microbiology
    2017 - 2019
  • Università degli studi Roma TRE
    Bachelor's degree, biology
    2014 - 2017

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