Marie-Josée Rocheleau

Tuteur privé Sciences et Chimie at SOSprof SOSteacher
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Contact Information
us****@****om
(386) 825-5501
Location
St-Hyacinthe, Quebec, Canada, CA
Languages
  • English Native or bilingual proficiency
  • French Native or bilingual proficiency

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Experience

    • Canada
    • Education Administration Programs
    • 1 - 100 Employee
    • Tuteur privé Sciences et Chimie
      • Feb 2023 - Present

    • Canada
    • E-learning
    • 1 - 100 Employee
    • Pigiste, Concepteur contenu pédagogique
      • Nov 2021 - Jan 2023

    • Canada
    • Primary and Secondary Education
    • 200 - 300 Employee
    • Enseignante Science et Technologie
      • Jan 2021 - Oct 2021

    • Analytical Chemist
      • Jan 2020 - Jan 2021

    • France
    • Environmental Services
    • 700 & Above Employee
    • Quality Control Coordinator
      • Jun 2018 - Jan 2020

    • Netherlands
    • Food and Beverage Manufacturing
    • 700 & Above Employee
    • Chemist
      • Nov 2017 - May 2018

    • Canada
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Analytical Scientist
      • Feb 2017 - Oct 2017

    • Canada
    • Hospitals and Health Care
    • 700 & Above Employee
    • Biochemist
      • Jul 2016 - Sep 2016

      Analysis of clinical samples by HPLC, UPLC and LC-MS, including sample process by SPE and liquid-liquid extraction.. Analysis of clinical samples by HPLC, UPLC and LC-MS, including sample process by SPE and liquid-liquid extraction..

    • Analytical Chemist, R&D
      • Oct 2013 - Dec 2015

      General analytical support of R&D projects. Develop and validate analytical methods (HPLC, UPLC, LC-MS, GC) for chemical intermediates and drug substances. Documentation management: Procedures-SOP, protocols, method and validation reports, certificate of analysis. General analytical support of R&D projects. Develop and validate analytical methods (HPLC, UPLC, LC-MS, GC) for chemical intermediates and drug substances. Documentation management: Procedures-SOP, protocols, method and validation reports, certificate of analysis.

    • Canada
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Analytical Research Scientist and Quality Control
      • Aug 2011 - Sep 2013

      Develop and validate analytical methods for drug substances and products. Perform transfer of analytical methods Analytical support for stability and toxicology studies by HPLC. Bioanalytical analyses of steroids (estrogen, testosterone, DHEA) by LC-MS. Review laboratory notebooks and documentation. Documentation management: Procedures-SOP, protocols, method and validation reports, certificate of analysis, and OOS results. Develop and validate analytical methods for drug substances and products. Perform transfer of analytical methods Analytical support for stability and toxicology studies by HPLC. Bioanalytical analyses of steroids (estrogen, testosterone, DHEA) by LC-MS. Review laboratory notebooks and documentation. Documentation management: Procedures-SOP, protocols, method and validation reports, certificate of analysis, and OOS results.

    • Canada
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Senior consultant
      • Oct 2010 - Dec 2010

      Offering professional training and expertise in pharmaceutical and analytical development. Offering professional training and expertise in pharmaceutical and analytical development.

  • LABORATOIRES OMEGA LTEE
    • Montreal, Canada
    • Manager Quality Control, Analytical Oncology Laboratory
      • Aug 2007 - Sep 2010

      Project Management in collaboratoration with Validation and Production Group, Regulartory Affairs and QA. Setting up the activities of a laboratory (formulation and analytical chemistry) Installation, qualification and troubleshooting of analytical equipment Hiring and training of laboratory personnel Review laboratory notebooks and documentation. Writing up procedures, protocols, method and validation reports Development and validation of analytical methodologies to test new generic drugs (small molecules and peptides). Show less

    • United States
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Researcher Investigator
      • Oct 1997 - Aug 2007

      (Supervisor, Analytical Method Development) Pharmaceutical and analytical method development for new drug substances and products. Project management on new drug development teams. Supervision of a team of junior chemists. . (Supervisor, Analytical Method Development) Pharmaceutical and analytical method development for new drug substances and products. Project management on new drug development teams. Supervision of a team of junior chemists. .

Education

  • McGill University
    Doctor of Philosophy - PhD, Analytical Chemistry
  • Université de Sherbrooke
    Bachelor's degree, Chemistry
  • Toxicologie des medicaments et agro-alimentaire, U. de Montréal
    Toxicologie et analyses du risque
    1996 - 1997
  • Clinical Research Training Centre, CRA School
    Clinical Research Professional Certification Program

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