Location:
Visp
Contract Period:
02/02/ /08/2026
Duration:
6 months *
Workload:
100%
Remote:
Up to 2 days per week
Language:
English required; German is a plus
Join our client's biopharmaceutical manufacturing team and contribute to the production of high-quality active ingredients for clinical and commercial use. This is an exciting opportunity to work in a cutting-edge environment while ensuring compliance with cGMP and safety standards.
Key Responsibilities
Lead project tasks in method development, implementation, transfer, and validation
Write and review test instructions, analytical methods, plans, and reports
Double-check and release raw data and analysis results in LIMS
Provide specialist laboratory support, including troubleshooting
Process CRs, DRs, investigations (SST, OOX, etc.), and CAPAs
Independently plan, execute, evaluate, and document assigned tasks and projects
Ensure compliance with ISO, GMP, and safety standards
Data Review experience is essential
Your Profile
PhD in biotechnology, biochemistry, pharmaceuticals, or related field with 1+ year experience
OR MSc in a relevant field with 2+ years in a laboratory/scientific role
Hands-on experience with ELISA (relative potency) and qPCR (development/validation)
GMP experience is a strong advantage
Interested?
Apply now with your CV.
Please note:
Only candidates with the
legal right to work in Switzerland
can be considered. This includes:
Swiss/EU/EFTA citizens
Holders of a valid Swiss work permit