Responsibilities of the job include:


  • Ensure the quality of QC equipment validation
  • Maintain compliance of equipment validations with regulatory standards
  • Ensure compliance (cGMP, local standards, guidance) at the validation level: Equipment, facilities, utilities and processes controls
  • Edit validation plans (PV) in accordance with the "change control" and "technical change description"
  • Assist, on request, QA deviation unit on cause and impact investigations
  • Support QA in change control & CAPA management in QC unit
  • Approve specific primary validation documents QC (SOP ...)
  • Approve specific documents of "change control" for validation QC
  • Carry out validation audits L2 and audits L1



  • Scientific training of the type Engineer or university (Bac + 5) in biotechnology, agronomy, chemistry, pharmacy
  • A first experience in the pharmaceutical industry, in production or QC testing process
  • Good knowledge of English (written and spoken) and French mandatory
  • Knowledge of GMP
  • Good writing skills
  • Good written and oral communication
  • Team Work and in field work




Activated at 06/20/2019
Locations Belgium
Category Consultants
Contact Victor Mauvady
Reference AD001377