CQV Coordinator (JO015421) Visp, Switzerland

As part of the CQV Team reporting to the CQ Manager main responsibilities and tasks of the incumbent includes but are not limited to:


  • Attendance at Factory Acceptance Tests for key process equipment
  • Execution of Walk Down of mechanically complete (MC) systems
  • Execution of Installation Verification (IQ)
  • Execution of Operational Verification (OQ)
  • Compliance with schedule
  • Safety Compliance

 Qualification & Experience Requirements

  • Education (minimum/desirable): Minimum BS or equivalent in Engineering or Science - preferably in Automation, Chemical, Mechanical or Pharmaceutical Engineering.
  • Experience in Commissioning and Qualification of Clean Utilities and gasses.
  • Experience in Commissioning and Qualification for the following equipment:
  • Single Use Mixers.
  • Tangential Flow Filtration.
  • COTS (freezers, fridges, probes (pH and UV))
  • Languages: English – Essential fluent in speaking and writing. German – advantageous.
  • Experience: Minimum 10 yrs.
  • Broad knowledge of engineering disciplines, commissioning, compliance, qualification and validation.
  • Excellent knowledge of Validation processes (IQ/OQ/PQ) and current regulatory requirements related to E2500 and ISPE 2004.
  • Experience working within a GMP manufacturing environment.