Tasks

  • Maintenance and improvement of the quality system
  • Preparation of batch releases including batch record Review
  • Processing of GMP relevant issues and activities
  • Processing and approval of GMP documents
  • Processing of modifications (change control), deviations, CAPAs, OOSs, Complaints
  • Supplier Quality Management: Supplier qualification overviews
  • Creation and revision of SOPs
  • Creation of the Annual Product Quality Review
  • Conducting of internal audits / support during the inspections

PROFILE

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