• Validation Master Plan (VMP)
  • Qualification of equipment and utilities
  • Risk Management
  • Specification and Risk Analyses Writing (FRA)
  • Protocol Writing (DQ, IQ, OQ, PQ, FAT, SAT) and tests
  • Qualification reports
  • Communication with suppliers
  • GMP Compliance


  • Engineer diploma or equivalent in pharmaceutical or Biotechnological field
  • Good Knowledge in Qualification
  • GMP Experience
  • Willingness to work in an international environment
  • English and German spoken and written