Scientist QC

Location: Visp
Contract Period: 02/02/2026 - 01/08/2026
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