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Hector Fabian Castro is a seasoned analytical chemist with over 20 years of experience in laboratory analysis, method development, and technical writing. He holds a BSc in Chemistry from the University of Buenos Aires and has worked in various industries, including pharmaceuticals and healthcare. Castro is certified as a Chemist by the Ordre des chimistes du Québec.

Credentials

  • Chemist, Ordre Chimistes Québec
    Membre de l'ordre des chimistes du Quebec
    Oct, 2009
    - Apr, 2026

Experience

  • Groupe PARIMA
    • Montreal, Quebec, Canada
    • Equipment and Instrumentation Specialist
      • Aug 2022 - Present
      • Montreal, Quebec, Canada

  • Loop Industries
    • Terrebonne, Quebec, Canada
    • Procurement , Health and Safety in Laboratory Agent
      • Nov 2021 - Present
      • Terrebonne, Quebec, Canada

    • R&D Laboratoty analyst
      • Jan 2015 - Present
      • Candiac

      Analytical method development.Validation of chromatographic and non chromatographic methods.Technical writing. Manage R&D Laboratory calibration program

    • Research and Development Laboratory Analyst
      • Jan 2012 - Present

      Analytical method development.Validation of chromatographic and non chromatographic methods.Technical writing.

    • QC Chemistry Laboratory Analyst
      • Oct 2010 - Dec 2011

      Quality Control of raw materials and finished products, according to USP, BP and CGMP regulations.

  • Groupe PARIMA Inc
    • Saint L:aurent
    • Chemist,R&V Scientist at Groupe Parima
      • May 2018 - Nov 2021
      • Saint L:aurent

      Laboratory health and safety .Development and validation analytical methods.Technical writting.

    • R&D Analyst
      • Oct 2003 - Dec 2009

      Stability and pharmaceutical analysis of finished drug product according to ICH regulations.High Performance liquid chromatography tests,Finished drug products dissolution/degradation profile.Deviation report writing and non -conformity identificationNormalized operative laboratory procedures revision and correction.

    • GMP coordinator
      • Jan 1998 - Jan 2003

      GMP internal and external audits execution.Technical writing.Employees trainingDesign and qualification of a pharmaceutical water system (quality USP 25).Validation protocols writing.

    • Instrumentation supervisor
      • Jan 1993 - Jan 1998

      Corrective/preventive analytical instrument UV-Vis, HPLC, FTIR, KF maintenance Analytical method development, process validation.Pharmaceutical analysis.Instruments calibration and verification.Manuals and technical sheets writing.

    • Laboratory technician
      • Jan 1987 - Jan 1993

      Liver enzyme analysis, protein electrophoresis, electrolyte determination in biological fluids.Laboratory employees training and technical support,

    • Laboratory technician
      • Jan 1986 - Jan 1987

      Medicines quality controlBioavailability study with HPLC methods.

    • Production Technician
      • Jan 1986 - Aug 1986

      Pharmaceutical ProductionPénicilline V and Erythromicyn manufactureLiquid and solid dosage forms production.

Education

  • 2015 - 2016
    Université du Québec en Abitibi-Témiscamingue
    Health and Safety at work certificate, HSW
  • 2006 - 2009
    Université de Montréal
    Dess Pharm. Development., Pharmacy
  • 1998 - 1998
    Universidad Nacional de San Martín
    Diploma, Quality Systems Manager
  • 1996 - 1997
    University of Buenos Aires
    Diploma, Health and Safety at workplace
  • 1985 - 1993
    University of Buenos Aires
    BSc, Chemistry
  • 1978 - 1983
    ENET N 1 Dr Ernesto Longobardi
    Technician, Chemistry

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Industry Focus. “Pharmaceutical Manufacturing”

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