Dr Tatiana Verissimo

Senior Scientist at Glass Pharms
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Contact Information
us****@****om
(386) 825-5501
Location
Maiden Bradley, England, United Kingdom, UK
Languages
  • Português Native or bilingual proficiency
  • Inglês Full professional proficiency

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Danielle Carvalho

Tatiana é uma analista atenciosa e dedicada! Possui boa criticidade analítica e tivemos sempre uma ótima interface acerca das análises físico-químicas.

Waleska Kerllen Martins

Tatiana é uma profissional dedicada, de fácil convívio e atenta à equipe que integra. Perfil colaborativo e com uma resiliência ímpar. A nossa interação e convivência no Instituto de Química da USP sempre foi amistosa, feliz e colaborativa. Agradeço imensamente a confiança e parceria!!!

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Credentials

  • Leading and Motivating People with Different Personalities
    LinkedIn
    Nov, 2022
    - Nov, 2024
  • Técnicas de Comunicação Interpessoal
    LinkedIn
    Oct, 2022
    - Nov, 2024

Experience

  • Glass Pharms
    • United Kingdom
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Senior Scientist
      • Jul 2023 - Present

      - Responsible for quality control activities including sampling and testing using a range of instrumentation; - Responsible for process development; _ To elaborate, review SOPs according GMP. - Responsible for quality control activities including sampling and testing using a range of instrumentation; - Responsible for process development; _ To elaborate, review SOPs according GMP.

  • União Química Farmacêutica Nacional
    • Brazil
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Development Analyst
      • Jan 2023 - Jun 2023

      - To work with Change controls (CM), CAPAs. - To write Procedures, specifications. - To replicate helping in update, to elaboration and to reviewing standard operating procedures (SOPs) of the area, multiplying the knowledge when necessary. - To elaborate with reports about elemental impurities following ICH Q3D using DMF s. - To work with Change controls (CM), CAPAs. - To write Procedures, specifications. - To replicate helping in update, to elaboration and to reviewing standard operating procedures (SOPs) of the area, multiplying the knowledge when necessary. - To elaborate with reports about elemental impurities following ICH Q3D using DMF s.

  • LIBBS FARMACÊUTICA LTDA
    • Brazil
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Analytical Methods Development Analyst
      • Sep 2020 - Jul 2022

      •To develop and to pre-validate (compendial and non-compendial) analytical methods throughout the product life cycle, aiming to identify and to implement process improvements that will reduce cycle time to test and release products. To provides project support for new product development which requires a close working relationship directly with customers as well as suppliers. •To assist in the failure investigations within other groups and design investigation protocols and suggest corrective action, and to improve analytical methods for portfolio maintenance, if necessary.•To act in the construction of the technical rationale for the unequivocal identification of organic impurities.•Stability and forced degradation studies according to current legislation.•To evaluate suppliers (Vendor) through physical-chemical analysis and Drug Master File (DMF) for submission of finished product or supplier change according to the regulatory agency.•To report the non-conformities/quality deviations detected, providing the pertinent information for evaluation and decision making.•To write and to review technical data, documents, SOPs, deviations, change control programs and cGMP guidelines, multiplying the knowledge when necessary.*To offer support to the maintenance and supply department by means of the necessity of interventions in the laboratory equipment.•To perform the analysis conference, critically evaluating all documents and records generated, the rationale used, the calculations and conclusions obtained.•To write and to review analytical methods, deviations, protocols, SOPs and any other technical documents as required.•To audits and to verifies results, including but not limited to, calculations in notebooks/logbooks and results in reports to check for accuracy and integrity of data. Show less

    • Quality Control Analyst
      • May 2019 - Sep 2020

      • To perform physical-chemical analysis of finished products, aiming at the approval of batches of all drugs in the industry following cGMP, performing the validation, as well as the treatment in cases of deviations, considering the definitions of the technical reports. • Laboratory maintenance and housekeeping, self-inspections and stock control; supporting the re-order systems and communicating with key suppliers..• Ensuring training status is compliant with matrix requirements and assisting in training other laboratory staff.• To manage data and results of the area in SAP system, checking all the analysis and reports for transfer in the system. • To audits and to verify results, including but not limited to, calculations in notebooks/logbooks and results in reports to check for accuracy and integrity of data.Main achievements:Participation in the internal project of the area of process change, assisting in the review of process flow, aiming to optimize processes and equipment use, increasing productivity and accuracy.Performance in the implementation of the cell analysis flow. Show less

  • Quest Diagnostics
    • United States
    • Hospitals and Health Care
    • 700 & Above Employee
    • Specialist R&D
      • Apr 2018 - Mar 2019

      • To approve of reagents and preparation of standard solutions used in laboratory routine, monitoring of external calibration and intermediate verification of equipment, building parameter deviation reports, preparation of standard solutions.• To write and to review SOPs, developing new methodologies with participation in the international accreditation (CAP - College of American Pathologists) and ISO 17025 accreditation.• Management of the processes of the Warehouse area, controlling the raw materials and supplies for the laboratory, defining the need for purchases.• Interface in synergy with other areas, following the traceability and data integration of the Unit, quality, and controls, searching for improvement opportunities, aiming the optimization of procedures.• Responsible for building samples and tests for product stability with more robust and safe tests.• Consulting processes of the other areas of the business as from material capturing, documentation registration, extraction, screening and validations of the materials for approval.• Governance of the research and validation of supplies to immunoassay (ELISA).• To manage the results and KPI's of the Unit, evaluating performance and quality, proposing actions for continuous improvement, presenting the results to the laboratory management and quality manager.• Focal point in internal audits, creating materials, procedures and conducting training in cases of non-compliance.• To give trainings related to procedures of the areas, reinforcing the values, mission and culture of the company, such with diverse themes as: water quality, pipetting among others.Main Result.Participation in the accreditation process of ISO 17025, surveying all the equipment, qualification, validation, calibration. definition of qualification parameters and acceptance of this equipment, ensuring the processes within the requirements for certification. Show less

    • FORENSIC SCIENTIST II
      • Sep 2017 - Mar 2018

      • Focal point of structuring the branch, performing the assembly standardization within the requirements and methodology of the U.S. headquarters and accreditation for CAP (College of American Pathologists), validation of internal processes. In this period I spent one month in Lenexa, Kansas to training.• Capacity building and leadership of the area with an average of 3 professionals, training the procedures and managing the performance and quality of the deliveries.• To perform analysis in LC-MS/MS and GC-MS/MS, control of area indicators and methodology transfer and validation with the other professionals of the Unit. To perform initial review the results. Main Result:Responsible for the project of methodology transfer from the USA to the Brazil unit, methodology validation within the local needs and current regulations, making the necessary adaptations when necessary. Show less

  • USP - Universidade de São Paulo
    • Brazil
    • Higher Education
    • 700 & Above Employee
    • Doctorate in Biological Sciences (Biochemistry)
      • Feb 2012 - Nov 2018

      USP is as second-best university in Latin America according to Quacquarelli Symonds (QS) Latin America Ranking (2022). During my PhD i worked with synthesis of superparamagnetic nanoparticles and their cellular internalization in cellular medium. In the development of this doctorate, I work with organic and inorganic synthetic route, preparation of solutions, characterization and quantification using equipment for characterization as infrared spectrum (FTIR), elemental analysis, nuclear magnetic resonance (NMR), liquid chromatography (HPLC, TLC) and gas chromatography (GC), mass spectrum (MS/MS), atomic absorption, transmission electron microscopy (TEM) and scanning electron microscopy (SEM), dynamic light scattering. I also develop work with cell culture, evaluation of cytotoxicity of drugs, sample preparation for confocal microscopy, cell viability. For all the experiments I wrote of scientific reports, calculations and statistics, also I made the presentations about the results obtained it. Show less

  • University of Ottawa
    • Canada
    • Higher Education
    • 700 & Above Employee
    • Visiting Research/ Internship
      • Jul 2015 - Jul 2016

      I went to develop niobium nanoparticle synthesis in a group with great knowledge of metal nanoparticle synthesis with applications in catalysis and biological applications. In this university under the supervision of Professor Juan Cesar (Tito) Scaiano, I had the opportunity to work with photochemical synthesis methodology for niobium and iron magnetic nanoparticles, as well as the characterization and toxicity evaluation of nanoparticles in cells. I went to develop niobium nanoparticle synthesis in a group with great knowledge of metal nanoparticle synthesis with applications in catalysis and biological applications. In this university under the supervision of Professor Juan Cesar (Tito) Scaiano, I had the opportunity to work with photochemical synthesis methodology for niobium and iron magnetic nanoparticles, as well as the characterization and toxicity evaluation of nanoparticles in cells.

  • Universidade Estadual Paulista Júlio de Mesquita Filho
    • Brazil
    • Higher Education
    • 700 & Above Employee
    • Degree Scientific Training
      • Aug 2009 - Dec 2010

      The work was to cultivate fungi on solid medium and, to evaluate the fungus for its potential in cellulose degradation for second generation ethanol generation. The work was to cultivate fungi on solid medium and, to evaluate the fungus for its potential in cellulose degradation for second generation ethanol generation.

Education

  • University of São Paulo
    Doctorate, Biological Science - Biochemistry
    2011 - 2018
  • MBA USP/Esalq
    Master of Business Administration - MBA, Project Management
    2019 - 2020
  • Escola EDTI
    White Belt, Project Management
    2019 - 2019
  • Universidade Estadual Paulista Júlio de Mesquita Filho
    Bachelor's Degree, Chemistry
    2006 - 2011
  • CDPI Pharma
    Pharmacy Administration and Pharmacy Policy and Regulatory Affairs, Affairs Regulatory - Industrial Professional Development Program
    2022 - 2023

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