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Experiences

Current Experience

  • Trainee industrial pharmacist - Qualified Person


    Since August 2015
    6 month traineeship as part of the Qualification of becoming qp in the eu. department: qc - raw materials -acting as study Director in a method Validation and Verification project concerning new raw materials. main responsibilities are writing Validation and Verification protocols and reports for the identification methods of compendial and non-compendial raw materials, drafting work instructions when methods aren't in place and being a liaison between the qc analysts and the project Coordinator/management. -writing SOP/work instruction for identification of raw materials with a portable raman spectrometer outside of the Validation project. -reworking Training material of practical Training for procedures performed in the qc Lab. -reviewing material Qualification plans and verifying whether the plans are in accordance with the urs and the applicable pharmacopoeia (ph. eur., usp, jp). reviewing subsequent Qualification reports and resource sheets. Qualification as Trainer within genzyme successfully completed: -ad hoc Trainer: theoretical Training to small groups and individuals -ojt Trainer: practical Training to small groups and individuals 6 month traineeship as part of the qualification of becoming QP in the EU. Department: QC - Raw materials -Acting as study director in a method validation and verification project concerning new raw materials. Main responsibilities are writing validation and verification protocols and reports for the identification methods of compendial and non-compendial raw materials, drafting work instructions when methods aren't in place and being a liaison between the QC analysts and the Project Coordinator/management. -Writing SOP/work instruction for identification of raw materials with a portable Raman spectrometer outside of the validation project. -Reworking training material of practical training for procedures performed in the QC lab. -Reviewing material qualification plans and verifying whether the plans are in accordance with the URS and the applicable pharmacopoeia (Ph. Eur., USP, JP). Reviewing subsequent qualification reports and resource sheets. Qualification as trainer within Genzyme successfully completed: -Ad Hoc trainer: theoretical training to small groups and individuals -OJT trainer: practical training to small groups and individuals

Past Experience

  • adjunct apotheker

    February 2014 --- August 2014

  • adjunct apotheker

    December 2011 --- December 2013

Personality

Self Assessment :
Analytical thinkingCritical thinkingInterest in knowledgeWillingness to compromiseFlexibility

Knowledge

Self Assessment :
Analytical Method ValidationcGMPMicrosoft OfficePharmaceutical IndustryQualificationTraining
LinkedIn Assessment :
Microsoft OfficeMicrosoft ExcelMicrosoft WordPowerPointLife SciencesGMPAnalytical Method Validation

Education

  • Master's degree in Industrial Pharmacy from Universiteit Antwerpen in 2015
  • Bachelor/master in Pharmaceutical Sciences - Drug development from Universiteit Gent in 2011

Languages

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

Work Preferences

  • Positions I am interested in:
    Qa
  • Locations I am interested in:
    Antwerp, Belgium Belgium
  • Work From Home:
    No
  • Work Regime:
    Permanent position
  • International:
    No

Area / Region

Antwerp, Belgium

Others

Driving License
  • Yes

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