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Paul GuillotPG

Paul Guillot

Regulatory Quality Consultant - cosmetics / agro

€750/day
La Rochelle, FR
8-15 years

Average response time: 1 hour

Freelancer profile translated to English.
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About Paul

I have over 12 years of experience in quality within demanding industrial environments in France and Canada, in the fields of cosmetics, pharmaceuticals, and agri-food. Curious, dynamic, rigorous, and flexible, I enjoy taking on new challenges to improve internal systems and bring my expertise in continuous improvement. With a Master's degree in analytical chemistry, I like to listen, analyze, and understand before proposing solutions to problems using methods and tools.
  • French

    Native or bilingual

  • English

    Native or bilingual

  • Spanish

    Conversational

Remote only
Primarily works remotely

Experience

  • SAS DOROGA
    REGULATORY COMPLIANCE QUALITY CONSULTANT
    E-COMMERCE
    September 2025 - Today (9 months)
    Regulatory support for product launches under the food supplement status in France and 9 European countries.
    Improvement of the subcontracting and contract management process, quality charter, and specifications.
    Réglementation alimentaire Lancement de produit Gestion de projet Cahier des charges
  • SV Labs
    QUALITY CONTROL MANAGER
    FASHION AND COSMETICS
    August 2024 - July 2025 (11 months)
    Brampton, ON, Canada
    • Supervision of the Quality Control team (5 people) for the quality control and release of bulk and products: 65 batches per week - 20 tanks - 25 filling lines.
    Management of Non-conformities, internal audits, process improvement, cleaning validation, FDA audits, laboratory management.
    Conformité réglementaire Amélioration des processus Contrôle qualité ISO 22716 cGMP
  • Biolab
    Associate in R&D Quality Assurance
    PHARMACEUTICALS INDUSTRY
    January 2024 - August 2024 (7 months)
    Mississauga, Canada
    Deployment of Biolab's quality management system for Pharma R&D in Canada.
    - Implementation of R&D compliance activities in accordance with GMP, GLP, GCP, Biolab policies, SOPs, and procedures.
    - Review and approval of documents to ensure their regulatory compliance and submission.
    industrie pharmaceutique Conformité réglementaire BPL Amélioration des processus R&D pharma

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Education

  • Master
    Master
  • Master Analytical Chemistry and
    Quality (CAQ)
    2012
    Master Chimie Analytique et

Skill set

Categories