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CSV Expert

CSV ExpertDoes the pharmaceutical industry appeal to you? Do you have experience with Computerized System Validation?Then do not stop reading, this offer might interest you!
Staat 60 dagen op Jobat.be

CSV Expert

Organisation

Our client is active in the pharmaceutical industry in Brussels.

Functieomschrijving

Responsibilities

  • Perform initial & periodical Computerized System validation for all GMP equipment at site (production & QC lab) 21 CFR Part 11
  • Review and approve risk assessment link to CSV
  • Performed routine Calibration & qualification activities
  • Ensure that all activities are performed according to the schedule
  • Ensure that all activities are properly documented
  • Write qualification and validation protocols and reports and other documentation related to the activities
  • Investigate deviations and execute CAPAs
  • Define and execute improvement projects and initiatives
  • Participate in customer and authority audits
  • Can be involved in other process validation activities

Profiel

Your Profile

  • You have a master degree in Biology/(Bio-)Engineering/Automation or equivalent
  • You have a relevant qualification & validation experience in the pharmaceutical/agro-food industry
  • You have experience in Computer System Validation
  • You are fluent in French and English
  • You have excellent communication skills
  • You are stress resistant
  • Risk analysis thinking

Keywords: CSV, risk assessment, CAPA, deviations, GMP, pharma

Aanbod

Offer

Our client offers you a new challenge in a dynamic industry with a competitive package.

Interested? Do not hesitate and apply for this wonderful opportunity! Any questions? Contact Diane Louppe: 02/389.11.76 or

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    Kenmerken

    Vereisten

    • Academische Bachelor

    Aanbod

    • Onbepaalde duur
    • Voltijds

    Solliciteer voor

    • 6 september

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