Experience

• 

  Sterinova

  • Canada
  • Pharmaceutical Manufacturing
  • 1 - 100 Employee

  • R&D manager, analytical and pharmaceutical development

    • May 2023 - Present

    Supervise analytical and pharmaceutical development staffOptimize development processManage deadlines and deliverables

  • R&D supervisor, analytical development

    • Aug 2022 - Apr 2023

    Supervise method development in the R&D group.Manage analytical method validation with external laboratory.Implement new proceduresSupport analytical method transfert from R&D group to QC group.

  • R&D Associate, Analytical method development and validation

    • Apr 2018 - Aug 2022

    Management of method development and analytical validation with external laboratories .Review and approval of protocol and analytical method validation report.Support to answer Health Canada request regarding analytical methods

• 

  Sandoz, Canada

  • Boucherville , Qc, Canada

  • Scientist, analytical method development and validation

    • 2015 - 2018
    • Boucherville , Qc, Canada

    Develop new analytical methods on pharmaceutical components. Participate to the project meeting and bring analytical expertise. Solve analytical problems encountered and provide support as needed. Validate the new methods according to the standards established by the company

• 

  Montreal University, Veterinary medicine faculty

  • Saint-Hyacinthe ,Qc , Canada

  • Chromatography laboratory manager

    • 2003 - 2015
    • Saint-Hyacinthe ,Qc , Canada

    Perform analyzes for diagnostic services such as; selenium, vitamins, mycotoxins and antiepileptic drugs, by liquid chromatography and mass spectrometry. Participate in various research works (mycotoxins, vitamins, selenium, omega 3, catecholamines, neurotransmitter, glucosamine, estradiol, amino acids, vitamin 25OH D3) Train and assist graduate students.

• 

  EZEM Canada

  • Specialist, Analytical method development and validation

    • 1999 - 2003

    Develop, improve and validate the analytical methods for the quality control laboratory, according to GLP, FDA and ICH standards. Qualify the QC instruments (OQ / PQ / PV). Write use and maintenance procedures and other SOP.

  • QC Analyst

    • 1995 - 1999

    Analyze raw material, finish product and stability product ( Cream, ointment, syrup, barium liquid preparation)Calibrate laboratory instrument such as pH meter, balance, GC, HPLC, etc

• 

  Rougier inc.

  • Chambly, Qc, Canada

  • Qc Analyst

    • 1990 - 1995
    • Chambly, Qc, Canada

    Analyze raw material and finish product as per USP, BP and GLP.