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Maroua Bhoury MelkiMB

Maroua Bhoury Melki

đź§Ş Pharmaceutical Development Engineer

€400/day
Montpellier, FR
3-7 years

Average response time: 1 hour

Freelancer profile translated to English.
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About Maroua

Industrial biology engineer specialized in pharmaceutical development, with 6 years of R&D experience in the pharma industry.
I have worked on projects of galenic formulation, process optimization, and scale-up, from the laboratory to the pilot scale, in an industrial environment.
My experience also covers R&D project management, stability studies monitoring, critical process parameter (CPP) and critical quality attribute (CQA) analysis, as well as contribution to technical documentation (CMC and regulatory dossiers).
Today, I provide technical and scientific support on pharmaceutical development missions, with a focus on formulation, literature review, and process optimization.
My goal is to provide reliable operational support to R&D teams, biotech, and pharmaceutical industries, in order to structure, analyze, and accelerate product development phases.
  • Arabic

    Native or bilingual

  • French

    Native or bilingual

  • English

    Fluent

Remote only
Primarily works remotely

Experience

  • PHARMA LABO
    Pharmaceutical Development Advisor & Sales Engineer
    RAW MATERIALS INDUSTRY
    February 2021 - November 2022 (1 year and 9 months)
    Tunis, Tunisia
    Technical support in pharmaceutical formulation and manufacturing
    Sourcing of pharmaceutical APIs and excipients
    Analysis of client needs and proposal of technical solutions
    Conducting market research and competitive analyses
    Participation in international trade shows (CPHI)
    API and Excipient Sourcing Galenic Formulation Formulas and Process Optimizations Industrial Transfer Consulting and Support
  • PHARMAGHREB
    Pharmaceutical Development Project Manager
    PHARMACEUTICALS INDUSTRY
    January 2018 - February 2021 (3 years and 1 month)
    Tunis, Tunisia
    Management of galenic development projects and formulation optimization.
    Design and execution of development and process optimization trials.
    Supervision of scale-up to industrial production.
    Monitoring of stability studies and development batch analyses.
    Contribution to regulatory dossiers (MA).
    Application of GMP and process validation.
    Galenic Formulation Industrial Transfer Process Validation Analysis and optimization of quality attributes (CQA) and process parameters (CQP/CPP) Formulas and Process Optimizations

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Education

  • Industrial biology engineer - Process engineering
    INSAT: National Institute of Applied Sciences and Technology
    2017

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