This role is ideal for the consultants with a solid expertise in Bioprocess Systems Qualification who are currently looking for a longer mission in a multinational biopharmaceutical company.
Start: as soon as possible
Duration: 12 months
- Creating qualification plans, reports, managing qualification tests
- Taking charge of deviations and CAPAs
- Responsible for coordination of the stakeholders and teams
- Preparation of the documentation for audits
- Support of the project and operation teams on the qualification activities
- In-depth knowledge of CQV on production equipment, cool systems and clean rooms
- Team player, good style of communication
- Excellent MS Office skills. Experience with COMOS, DMS, TrackWise, KNEAT and SAP is a big plus
- German/English fluent
If you think that you are a good fit, please don't hesitate to apply.