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Summary

I have a master in Chemistry from the Université de Namur and during my education, I worked with the following tools: IR spectroscopy, X-ray diffraction (XRD), Thermogravimetric analysis (TGA), Nitrogen adsorption, Transmission Electron Microscopy (TEM), Scanning Electron Microscopy (SEM), High-performance liquid chromatography (HPLC).

I have 7 years of experience in the R&D Department for a company specialized in infant nutrition. I am principally in charge of the following tasks:

  • Validation of the formulated products after production (organoleptic evaluation)
  • Responsible for the product labelling in accordance with the regulations in force (creation, checking and regular update of the designs in collaboration with the Marketing Department)
  • Responsible for the submission, follow-up and renewal of the registration files for current and new products
  • Handling of Customer complaints
  • Regular contacts with the suppliers and customers
  • Research and analyses of scientific documents – synthesis and internal communication

I am looking for new opportunities and particularly in the pharmaceutical field and I would like to offer my skills to a leading company in its sector. Accurate and organized, I am a trustworthy person with teamwork skills. I am looking for a position of responsibility that utilizes my skills and experience and I am keen to work in an environment where I can enrich my knowledge. My excellent listening and adaptability skills will certainly be assets.

Experiences

Current Experience

  • Scientific Support Officer
    Since May 2008

    FASSKA-PAR is specialized in the Formulation, Production and Marketing of Nutritional Products for humans and especially infants milk formulas and other food for babies & Adults.

    Two other ranges complete this large selection of products: Formulated Nutritional Supplements for pregnant women and breastfeeding women and replacement nutrition or nutritional supplements linked to specific pathologies such as kidney failure and diabetes.

    • Multi-purpose function in an international environment
    • Validation of the formulated products after production (organoleptic evaluation)
    • Responsible for the product labelling in accordance with the regulations in force (creation, checking and regular update of the designs in collaboration with the Marketing Department)
    • Responsible for the submission, follow-up and renewal of the registration files for current and new products
    • Handling of Customer complaints
    • Regular contacts with the suppliers and customers
    • Research and analyses of scientific documents – synthesis and internal communication

     

Personality

Self Assessment :
Attention to detailCollaborationCuriosityCritical thinkingReaction to stressProactivityOrganizationInterest in knowledgeFlexibility

Knowledge

Self Assessment :
R&DCAPAChemistryEnglishGMPHPLCGood Manufacturing Practice (GMP)ICH GCP guidelinesIt skillsLaboratoryMicroscopyMicrosoft ExcelMicrosoft OfficePowerPointQuality Assurance (QA)Registration of the productRegulatory affairsValidation

Skills and Expertise

Self Assessment :
Control data Lab scale batchesApprove Label Master SheetCollaborate with project teamData verificationWriting regulatory documentsWork under specific instructionsVerify dataValidate dataSolve problemsResearch at universitiesRegulatory submissionsRegulatory documentationQuality control processPrepare regulatory documentslifescienceLabeling compliance with local regulationsEnsure data consistencyFollow-up of quality assurance activities

Education

  • Master in Chemistry from Université de Namur in 2007
  • CESS in Sciences-Mathématiques from Communauté Scolaire Sainte-Marie Namur in 2002

Training and Certification

  • GMP in 2015 Training
  • Good validation practices in 2015 Training
  • Languages

    BrightOwl Assessment:
    Self Assessment:
    French
    Native
    English
    Professional Proficiency
    Dutch
    Elementary Proficiency

Work Preferences

  • Notice Period:
    13 weeks
  • Positions I am interested in:
    Regulatory Affairs Consultant Scientist Clinical Research Associate (CRA) Quality manager
  • Locations I am interested in:
    Brabant Wallon, Belgique
  • Work From Home:
    Yes, 0 to 3 days per week
  • Work Regime:
    Permanent position
  • International:
    No

Area / Region

Schaltin, Belgique

Others

Driving License
  • Yes