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Toulouse
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Laboratory equipment qualification engineer CSV - Pharma - Toulouse 

Our client is a renowned European consulting firm specialising in the life sciences industry. With a strong focus on quality, regulatory compliance, and project management, our client provides comprehensive solutions to help clients navigate the complex landscape of drug development, medical device manufacturing, and healthcare services.

Role:
  • You will join the team generating qualification/validation documents for computerized systems related to laboratory equipment on our client's site located in Toulouse.
  • Write documents related to the validation of computerized laboratory equipment systems (URS, Data Integrity Assessment, Risk Assessment, IOQ Protocol)
  • Support for managing qualification non-conformities (investigation, assessment, CAPA proposal)
  • On demand: Execution of qualification protocols in support of the team/Support of the CQV team to carry out qualification tests linked to the CSV.

Requirements: 
  • 5 to 10 years of experience in validation of computerized systems related to laboratory equipment
  • Experience in writing URS, risk assessment, IOQ protocol
  • Experience with the following equipment: Mass Spectrophotometer, Cellometer, electrophoresis, Infrared SPectrophotometer, colony counter, PCR, Protein simple analyzer, thermostatted enclosures

If this role is of interest to you, please apply now! 

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