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First, I want to Thank you for visiting my profile. You'll find everything about my studies, my professional career and in particular my professional goal...

Who am i?

 After a Specialized Master Degree "Biotechnology & Quality Approach", today I got 3 years experience in the pharmaceutical industry (Quality Assurance, Quality Control, Manufacturing-Quality).

What am I looking for?

 A new challenge where I can develop my professional skills.  To discover a new atmosphere where I can meet more professionals.  To represent a new driving force for a Pharmaceutical / Agroalimentary / Cosmetic / Chemistry industry.  To reach new targets by using new tools.  To learn how to improve my know-how.

What can I provide?

 My Knowlegde in the Quality Field, which includes :

Quality Risk Management - Quality inspection / Internal Quality Audit - Supplier's complaints - Change controls - C.A.P.A (Corrective Actions & Preventive Actions) - Annual Products Review - Cartography of the processes - Quality tools (Ishikawa's diagram - Pareto’s diagram - F.M.E.C.A - Control Cards – Experience’s Plans - Brainstorming) - Quality indicators - Pharmaceuticals GMP Guidelines - FDA standards - ISO 9001, ISO 22000, ISO 14001, HACCP.

I can also provide some of my modest skills which can be very useful in any new strategical position :

  • 4 Languages speaking : Arabic, French, English & Spanish. - Project Management (Planning, steering, ...).
  • Communication - Public Speaking - Team work - Leadership - Strictness - Extension's respect - Execution's quality.


Current Experience

  • Quality Assurance Executive
    Since March 2013
     Insure the Quality Assurance’s check points during all the manufacturing process and validate the interface between the Quality System and the other departments.  Analyze Quality Assurance requirement and develop quality solutions & processes for the internal audit implementation.  Coordinate and investigate the organisation’s incidents cases (CAPA).  Achieve lot’s files reviews and the monitoring of the preventives & correctives actions within the deadlines.  Realize proximity quality monitoring in the related departments and to set the recommendations to get under control the product’s quality all along the chain.  Monitor procedures application effectiveness, the technics inside the manufacturing working group and the respect of the good manufacturing / hygiene / recording practices.  Train and form newly recruited in their respective departments.

Past Experience

  • Quality Engineer - Internship
    February 2012 --- May 2012
     Monitoring and improving the Prerequisite Program in all the manufacture’s departments.  Aware the machine operators to respect the hygiene rules established by the manufacture and also by the quality department and train the new recruited operators to the hygiene rules.  Implementation of the Control Cards (shewhart) in view to highlight the sanitary security of the Ice cream manufacturing during all the year.

  • Quality Engineer - Internship
    July 2011 --- August 2011
    - Intern Quality Audit. - Initiation to the Prerequisite programs. - Track all kinds of malfunctions.

  • Quality Engineer - Internship
    February 2010 --- April 2010
    Quality & salubrity of the Marins habitats: Réalisation des études de zones au niveau des gisements coquilliers naturels et les sites conchylicoles et la surveillance bactériologique des zones de production conchylicole classées. - Analyse des échantillons (recherche et dénombrement d’Escherichia coli et recherche de présence ou absence de Salmonella) pour avoir la certification de l’accrédibilité des analyses microbiologiques. - Participation à la mise en place de process et d’outils de surveillance relative à l’apparition des biotoxines et du phytoplancton nuisibles ; - Participation à l’établissement d’un rapport sur l’état de l’environnement marin.


Self Assessment :
ISO 22000ISO 14001HACCP.Quality Risk Management Biochemistry Cell biology Negotiation Scientific writingBiotechnologyPharmaceuticals GMP Guidelines - FDA standards - ISO 9001ISO 22000ISO 14001HACCP.Pharmaceutical GMP GuidelinesDrug Safety and PharmacovigilanceEnvironmental ScienceGalenicsGMPHealthcare industryHealthcare ManagementHealthcareGood Distribution Practice (GDP)Good Laboratory Practice (GLP)Good Manufacturing Practice (GMP)Laboratory ManagementLeadershipmanagementManufacturingMicrobiologyMicrosoft ExcelMicrosoft OfficeMicrosoft PowerpointMicrosoft WordMicrosoft ProjectNegotiationNutritionOutlookOutsourcingPharmaceutical IndustryPharmaceutical DevelopmentPharmaceutical ManufacturingPharmaceutical SciencesPharmaceutical managementPowerPointQuality Assurance (QA)Quality AuditingQuality Control (QC)Quality ManagementQuality Management System (QMS)Quality SystemsRisk ManagementToxicologyValidationBiologyBPF
LinkedIn Assessment :
managementAssurance qualitGestion de la qualitMicrosoft OfficeBPFHACCPContrSecteur pharmaceutiqueMicrosoft ExcelSystNGMPgestion de projet

Skills and Expertise

Self Assessment :
Management Assurance qualité Gestion de la qualité Microsoft Office BPF HACCP Contrôle qualité Secteur pharmaceutique Microsoft Excel Système qualité Négociations GMP gestion de projet


  • Master's degree in Biotechnology & Quality Approach from Université Hassan II Mohammedia in 2012

Training and Certification

  • Area's treatement in a Pharmaceutical Manufacturing in 2015 Training
  • CAPA'S Treatement in 2015 Training
  • Languages

    BrightOwl Assessment:
    Self Assessment:
    Full Proficiency
    Professional Proficiency
    Professional Proficiency

Work Preferences

  • Notice Period:
    10 weeks
  • Work From Home:
  • Work Regime:
    Permanent position
  • International:

Area / Region

Casablanca-Anfa, Grand Casablanca, Morocco


Driving License
  • Yes