(m/f/d)
Urdorf
Start date: asap
Reference number: 873927/1
Manage Change Requests, CAPAs, and Non-Conformities
Execute established workflows for biotech development projects
Act as a key contact for all quality-related topics within the project team
Perform risk and hazard analyses, including FMEA
Conduct incoming inspections, in-process controls, and FATs
Maintain and manage the electronic Document Management System (eDMS)
Support the implementation of a supplier management process