(Senior) Technical Assistant CTM Analytics - Valneva


  • Setting up, transfer and validation of analytical GMP release and stability tests for multiple projects in the clinical development
    including preparation/completion of protocols and reports
  • Execution of diverse analytical procedures (e.g. ELISA, HPLC, cell based assays, etc.) as part of quality control testing of products /
    clinical trial materials according to defined standard operating procedures and protocols and in compliance with the same
  • Conduct on-time reporting according to the defined and trained document management standards including review and verification of
    analytical data
  • Preparation and review of GMP relevant documentation in English language (e.g. Deviations, Changes, SOPs)
  • Active participation in laboratory investigations and documentation thereof
  • Assume responsibility for laboratory equipment

Janine Kügle, LL.B, M.A.
E applications.hr.vie(at)valneva.com

Details Technical Assistant CTM Analytics - Valneva 1