Process Validation Specialist
Key information
- Publication date:15 May 2025
- Workload:100%
- Contract type:Temporary
- Language:English (Fluent)
- Place of work:Visp
For Lonza AG in Visp, Switzerland, we are looking for a Process Validation Specialist 100% in the pharmaceutical or biotech sector.
Key responsibilities
-
Design process validation strategy and prepare documentation per Lonza and regulatory standards
-
Support R&D during process characterization
-
Review and approve characterization documents
-
Assess and approve changes and deviations
-
Develop and maintain continued process verification plan
-
Review and approve Product Quality Reviews
Qualifikationen
-
Master's in science or engineering (e.g. Chemistry, Biotech)
-
Project management experience; MSAT/Quality/Operations preferred
-
Experience with cross-functional teams; regulatory exposure a plus
-
Basic knowledge of mammalian cell culture
-
Strong multitasking and communication skills
-
Fluent in English; German a plus
-
Hybrid: 2 days remote, 3 days onsite