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Summary

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 :

Experiences

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.  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.

Knowledge

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

Education

  • 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:
    Arabic
    Native
    French
    Full Proficiency
    English
    Professional Proficiency
    Spanish
    Professional Proficiency

Work Preferences

  • Notice Period:
    10 weeks
  • Work From Home:
    No
  • Work Regime:
    Permanent position
  • International:
    Yes

Area / Region

Casablanca-Anfa, Grand Casablanca, Morocco

Others

Driving License
  • Yes

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