The purpose of the position is to ensure manufacturing process (including equipment, methods, CSV) are appropriately qualified and validated while conducting review of related documentation and leading quality risk assessment and change management activities.
Position Requirements:
Engineer in Automation or Processes or Chemistry or Pharmaceutical technology or Mechanic,
3 years" experience in Equipment qualification in GMP/Pharmaceutical environment/ Quality Control of Pharma companies,
Deep knowledge of FDA and EU guidelines about Validation or Quality Control tests, lab instruments and validation,